KKORETREAT
TQ-021 · v4.2EN / ES01 / 12
Master technique guide · clinician

BiViDerma
technique guide.

A clinician-facing reference for injecting BiViDerma I, III, and V — covering product rheology, patient consultation, anatomical mapping, injection protocols by zone, post-treatment care, and adverse-event management.

Audience
Certified injectors
Last revision
March 2026
Revision cycle
Quarterly

Contents

02Product family — rheology & positioning
03Patient consultation framework
04Pre-injection preparation
05Anaesthesia options
06Upper face — temple, glabella, brow
07Peri-orbital — tear trough
08Mid-face — cheek, NLF
09Lower face — chin, jawline, marionette
10Lips — vermillion, body, cupid's bow
11Post-injection assessment & aftercare
12Adverse-event decision tree
Koretreat Market SAS · ARCSA-2023-3.3-0000041For clinical use only
KKORETREAT
TQ-021 · Technique guide02 / 12
Product family

Three densities. One scientific principle.

BiViDerma uses Multi-Layered Crosslinking (MLC) — three sequential cross-linking passes that capture a denser lattice inside a softer outer matrix. The result: hydration that stays where it's placed, with predictable rheology.

VariantHAG′CohesivityLiftLongevityIndication
BiViDerma I
Light · 30G TW
24 mg/ml 180 Pa 26 % Low 9 mo Lips, fine lines, tear trough, hydration
BiViDerma III
Medium · 27G TW · 25G cannula
24 mg/ml 320 Pa 62 % Medium 14 mo Mid-face, NLF, marionette, chin contour
BiViDerma V
High · 27G TW · 22G cannula
24 mg/ml 540 Pa 88 % High 18 mo Cheekbone, jawline, chin tip, deep volume

Storage

5–23 °C, ambient. No refrigeration required. Protect from direct sunlight. 24-month shelf life.

Lidocaine

All variants contain 0.3% lidocaine HCl for patient comfort. Verify allergy history before injection.

BDDE

Residual cross-linker < 2 ppm across all variants — within international safety thresholds.

Clinical · BiViDermav4.2 · 2026
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TQ-021 · Technique guide03 / 12
Step 01 · Consultation

Listen first. Inject last.

A structured 15-minute consultation prevents 80% of post-treatment disappointment. Photograph, document, and align expectations before opening a single syringe.

  1. History. Allergies (lidocaine, BDDE-class agents), prior filler exposure, current medications including anti-coagulants and aspirin, pregnancy or breastfeeding status, active skin infection, autoimmune disease, dental work pending in next 4 weeks.
  2. Expectations. Ask the patient to describe — not point at — what they want changed. Open-ended question: "If we did one thing today, what would have the biggest impact for you?" Listen for unrealistic goals (e.g. "I want to look like X").
  3. Photograph. Standardised lighting, neutral background, 0°/45°/90° angles, rested expression and animated expression. Without this you have no medico-legal baseline.
  4. Assess. Skin quality (Glogau scale), bone-loss pattern, fat-pad descent, asymmetry. Document on a face diagram — show the patient.
  5. Plan. Volume estimate per zone, product per zone, total syringes, indicative price. Schedule a touch-up review at week 2.
  6. Consent. Signed informed consent listing common risks (bruising, swelling) and rare risks (vascular occlusion, blindness). Patient initials each line.

Decline if

— Active herpes simplex or skin infection in the treatment area. — Patient under 18 (without specific legal context). — Body dysmorphic indicators or unrealistic expectations. — Pregnancy or breastfeeding. — Recent (< 2 weeks) dental work, vaccination, or another filler product in the same plane.

Clinical · BiViDermav4.2 · 2026
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TQ-021 · Technique guide04 / 12
Step 02 · Preparation

Mark, cleanse, anaesthetise.

Marking — patient upright

  • — Map gravity-dependent fat-pad descent.
  • — Mark vascular danger points: facial artery, infraorbital foramen, mental foramen, supratrochlear notch.
  • — Outline injection vectors with surgical pen.
  • — Show the patient in the mirror. Confirm.

Cleansing

  • — Remove makeup with micellar water.
  • — Cleanse with chlorhexidine 0.5% in 70% ethanol. Two passes.
  • — Avoid iodine-based preparations in the mid-face (staining, sensitivity).
  • — Allow 60 seconds to dry. Inject through a cleansed field only.

Tray setup checklist

  • BiViDerma syringe(s) — verify lot, expiry, integrity of packaging.
  • Cannulas in correct gauge(s) for the plan.
  • Needles 23G (entry pre-dilation), 27G, 30G.
  • Topical anaesthetic and remover.
  • Hyaluronidase 1500 U vial. Reconstitution solvent. Verify expiry.
  • Sterile gauze, cotton-tipped applicators.
  • Cold packs (clean, dry).
  • Camera ready. Consent form signed and visible.
Clinical · BiViDermav4.2 · 2026
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Step 03 · Anaesthesia

Comfort without compromise.

BiViDerma contains 0.3% lidocaine intrinsically. Topical and regional anaesthesia stack on top of this for sensitive zones — especially lips and tear trough.

TechniqueAgentOnsetBest forNotes
TopicalLidocaine 4% / prilocaine 2.5%20 minLips, tear trough, fine linesApply under occlusion. Remove fully before injection — residue compromises adhesion of dressings.
IceClean dry pack30 sCheek, NLF, marionetteHold against vector for 30 s immediately before puncture. Patient-titrated.
Infraorbital blockLidocaine 2% + epi (intra-oral)3 minTear trough, NLF, upper lipTrans-mucosal at canine fossa. 0.5–1.0 ml per side. Risk: vascular event, transient ptosis.
Mental blockLidocaine 2% (intra-oral)3 minChin, lower lip, marionetteTrans-mucosal at second-premolar root. 0.5 ml per side.
Vibration / distractionImmediateAll zonesGate-theory based. Cheap, effective, no drug burden.

Anaesthetic limit

Maximum lidocaine dose 4.5 mg/kg (without epinephrine), 7 mg/kg (with). A standard mid-face plan (intrinsic + topical + block) is well within this limit, but track carefully for combined-zone work or low-weight patients.

Clinical · BiViDermav4.2 · 2026
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TQ-021 · Technique guide06 / 12
Zone 01 · Upper face

Temple. Glabella. Brow.

Temporal hollows

Product
BiViDerma V
Tool
22G × 70 mm cannula
Entry
1 cm inferior to the zygomatic arch, lateral canthus vertical
Plane
Supraperiosteal (deep) or sub-galeal (superficial)
Volume
0.5–1.0 ml per side, divided into 2–3 fan vectors
Avoid
Middle temporal artery (runs ~1 cm anterior to tragus, deep)

Glabella — fine lines

Product
BiViDerma I (consider neuromodulator first)
Tool
30G × 13 mm needle, intradermal threading
Entry
Lateral end of each glabellar line
Plane
Mid dermis
Volume
0.05–0.15 ml total. Never bolus.
Avoid
Supratrochlear / supraorbital — retinal anastomosis. Stay superficial, retrograde only, < 0.05 ml per pass.

The glabella is a high-stakes zone

Most reported blindness events from filler injection involve the glabella or nasal dorsum. If the patient's primary concern is dynamic glabellar lines, neuromodulator is the safer first intervention. Reserve filler for static residual lines only, intradermal, threading retrograde with minimal volume.

Clinical · BiViDermav4.2 · 2026
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Zone 02 · Peri-orbital

Tear trough.

The tear trough rewards conservatism — over-correction is more disfiguring than under-correction. Use only the lightest product, pre-periosteal, in 0.05-ml aliquots.

Product
BiViDerma I — the only variant for this zone.
Tool
25G × 38 mm cannula. Sharp needle is acceptable only for experienced injectors using pre-periosteal serial puncture.
Entry
2 cm inferior to the lid margin, mid-pupil vertical. Pre-dilate with 23G needle.
Plane
Pre-periosteal — directly on bone. Anything above this risks Tyndall, lymphatic congestion, or visible product.
Vector
From entry point, advance cannula medial along the inferior orbital rim. Inject on retraction only, 0.05 ml every 5 mm.
Volume
0.2–0.5 ml per side total. Stop earlier than feels right.
Avoid
Infraorbital foramen (1 cm below the rim, mid-pupil). Stay deep to the orbicularis. Never inject superficial in this zone.

Patient selection

  • — Tear-trough deformity in the absence of lower lid bag.
  • — Adequate skin thickness (pinch test > 2 mm).
  • — No history of malar oedema.

Decline if

  • Festoon or lower-lid bag present.
  • Thin skin, prone to Tyndall.
  • Previous unsatisfactory tear-trough work elsewhere — dissolve first, treat later.
Clinical · BiViDermav4.2 · 2026
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Zone 03 · Mid-face

Cheekbone. Anterior cheek. NLF.

Zygomatic / malar projection

Product
BiViDerma V (structural) ± III (anterior blending)
Tool
25G × 50 mm cannula. 27G needle acceptable for periosteal bolus on the zygomatic apex.
Entry
Pre-jowl sulcus or anterior to the zygomatic arch
Plane
Supraperiosteal — directly on bone, deep to SMAS
Volume
0.8–1.5 ml per side. Bolus 0.2–0.3 ml on bone, then fan anteriorly with III in deep fat compartment.
Avoid
Transverse facial artery (parallel to zygomatic arch, 1 cm inferior). Stay on bone.

Nasolabial fold (NLF)

Product
BiViDerma III
Tool
25G × 50 mm cannula. Cannula strongly preferred — facial artery runs at the medial cheek base.
Entry
Cephalic to the fold apex, lateral to nasal ala
Plane
Deep dermis blending into SMAS
Volume
0.4–0.8 ml per side. Linear threading, retrograde.
Pearl
Soften the fold; do not erase it. Over-correction produces an unnatural lateral shelf.

NLF + glabella + nose = highest published occlusion sites

If the patient has had a prior occlusion in any of these zones, do not inject the same territory. Refer to a senior colleague.

Clinical · BiViDermav4.2 · 2026
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Zone 04 · Lower face

Chin. Jawline. Marionette.

Chin — projection & contour

Product
BiViDerma V
Tool
27G × 25 mm needle (mid-line periosteal bolus); 22G × 50 mm cannula for lateral blending
Plane
Supraperiosteal
Volume
0.5–1.5 ml total. 0.3–0.5 ml mid-line bolus + lateral blending.
Avoid
Mental foramen (vertical line below second premolar). Stay medial of foramen for the bolus.

Jawline

Product
BiViDerma V
Tool
22G × 70 mm cannula
Entry
Pre-jowl notch and gonial angle (two entry points per side)
Plane
Supraperiosteal
Volume
1.0–2.0 ml per side. Linear retrograde threading along the inferior mandibular border.
Pearl
Stop 1.5 cm posterior to the mental foramen on each side. Re-enter from the gonial angle for the posterior jaw — do not push a single thread across.

Marionette

Product
BiViDerma III
Tool
25G × 50 mm cannula
Entry
Lateral commissure
Plane
Deep dermis
Volume
0.3–0.6 ml per side
Clinical · BiViDermav4.2 · 2026
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Zone 05 · Lips

Vermillion. Body. Cupid's bow.

Lips show every error. Plan vectors before opening the syringe; never improvise on the table.

Vermillion border

Product
BiViDerma I
Tool
30G × 13 mm needle
Technique
Linear retrograde threading along the white roll
Plane
Submucosal, just deep to vermillion
Volume
0.1–0.3 ml per lip

Lip body (hydration / volume)

Product
BiViDerma I
Tool
30G × 13 mm needle, or 27G × 38 mm cannula for experienced injectors
Technique
Serial micro-puncture (0.02 ml per puncture) along the wet/dry junction
Plane
Submucosal
Volume
0.2–0.5 ml per lip

Cupid's bow

Tool
30G × 13 mm needle
Technique
Two precise punctate boluses, 0.02 ml each, at the philtral column tubercles
Plane
Submucosal
Volume
0.04–0.08 ml total

Lip ratios

Aim for an upper:lower lip ratio of 1:1.6 (golden) for European morphology. Asian and African lip morphology may target 1:1 to 1:1.3. Match the patient's facial proportions, not a single universal target.

Clinical · BiViDermav4.2 · 2026
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Step 04 · Post-injection

Assess, instruct, schedule.

Immediate assessment (5 minutes on the table)

  1. Patient upright. Reassess in natural light. Photograph mirror-image of pre-treatment angles.
  2. Animate. Smile, frown, purse. Identify any dynamic asymmetry.
  3. Gentle massage for even distribution — only where intended, never where contraindicated (tear trough, lip body).
  4. Capillary refill test in any zone of concern. > 2 seconds → reassess for occlusion.
  5. Cold compress 5 minutes before the patient leaves.

Patient instructions

Hand the patient the relevant aftercare PDF (AC-001 for lips, AC-002 if mid-face was treated). Walk through it before they leave. Confirm:

Documentation

In the patient record: lot numbers per syringe used, volume per zone, technique (cannula vs needle, gauge), anaesthesia used, immediate adverse events, post-procedure photographs, instructions provided, follow-up scheduled.

Clinical · BiViDermav4.2 · 2026
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Step 05 · Adverse events

Decision tree.

EventTimingFirst actionEscalation
Bruising0–7 dPressure, ice, arnica topicalPulsed-dye laser if persistent > 7 d
Swelling0–3 dCold compress, head elevationAntihistamine if > 3 d; steroid only if severe
Lumps / nodules2–14 d (early), 4 wk+ (late)Massage if early; reassureLate nodule → hyaluronidase + steroid; biopsy if persistent
Vascular occlusionImmediateSTOP. Hyaluronidase 200–450 U. Warm compress. Aspirin 325 mg.Hospital if > 4 h or any visual symptom
Visual symptomsImmediateSTOP. Call 24/7 hotline. Patient flat. Hospital transfer.Ophthalmology emergency
Infection3 d+Culture, oral antibioticsIV antibiotics + hyaluronidase if abscess
GranulomaWeeks–monthsDocument, photographIntralesional steroid + hyaluronidase + 5-FU
Tyndall (bluish)Days–weeksHyaluronidase to dissolveRe-treat in correct plane after 2 wk

Support contacts

+593 988 089 010

24/7 clinical hotline

farmacovigilancia@
koretreat.com

Reporting

  • — Within 48 h of any adverse event.
  • — ARCSA notification filed by Koretreat on your behalf.
  • — Maintain your local patient record per Ecuadorian regulations.

Disclaimer. This guide is a reference, not a replacement for certified training. BiViDerma practitioner certification is conducted quarterly by Koretreat — contact training@koretreat.com. Local regulation (Ecuador: ARCSA) may impose additional requirements. Practitioners are responsible for adherence to their jurisdiction's rules and their own clinical judgement.
Koretreat Market SAS · ARCSA-2023-3.3-0000041TQ-021 · v4.2 · 2026