TEOFIL Deep 1.1 ml

TEOFIL Deep 1.1 ml

TEOFIL (Teofil)

Medical device — hyaluronic acid dermal filler
  • CE certified (manufacturer brochure explicitly states CE certification for TEOFIL family).
  • Manufacturer claims ISO 13485 quality management compliance.
  • Manufacturer states HCCL™ manufacturing process and in House clinical testing (clinical trial data summarised in manufacturer brochure).
Monophasic HA dermal filler for medium-to-deep dermis / volume restoration

Description

TEOFIL Deep is a CE-certified, monophasic cross-linked hyaluronic acid (HA) filler manufactured using HCCL™ (Highly Completed Cross-Linking) technology. Formulated as a viscous, elastic gel for medium-to-deep dermal injection, Deep is intended to correct deeper folds, restore lost facial volume and enable lip augmentation. The product is supplied in a prefilled syringe (1.1 ml) and includes lidocaine for patient comfort.

Bnefits

  • Monophasic gel structure for consistent texture and smooth integration
  • HCCL™ advanced cross-linking technology (manufacturer claim) for stabilized 3D matrix and enhanced rheological properties
  • Contains lidocaine (0.3%) to improve injection comfort
  • 20 mg hyaluronic acid per ml concentration for volumising and hydrating effect
  • Packaged as ready-to-use prefilled syringe (1.1 ml) with needles included per product summary
  • CE marked and produced under ISO 13485 processes per manufacturer literature

Indications

  • Correction of deep facial folds and restoration of facial volume (e.g., nasolabial folds)
  • Lip augmentation and lip volumising
  • Facial contouring where medium-to-deep dermal placement is clinically indicated

Composition

  • Cross-linked hyaluronic acid (HA) — 20 mg/ml as stated in manufacturer product literature
  • Lidocaine — 0.3% (stated in product summary)
  • Cross-linking performed using HCCL™ technology (manufacturer description; exact cross-linker residuals not published)

Formulation

  • Monophasic hyaluronic acid gel with enhanced viscoelasticity intended for injection into medium-to-deep dermis
  • Supplied as 1 x 1.1 ml prefilled syringe (Deep variant) with needles included (manufacturer product summary lists 1 x 25G needle and 1 x 27G needle)
  • Sterile, single-use injectable device

Packaging

  • Typical pack: 1 x 1.1 ml prefilled syringe (Deep) in sterile single-use packaging; carton and leaflet included (pack contents listed in manufacturer brochure)
  • Needles included in the pack per product summary (exact needle gauges listed in manufacturer brochure)

Usage

  • For professional use only by qualified practitioners trained in injectable dermal fillers (manufacturer and distributor pages state professional use requirement).
  • Follow aseptic technique and local protocols for injection depth and technique; Deep is described for medium-to-deep dermal placement and lip augmentation per manufacturer guidance.
  • Use appropriate needle/cannula sizes as per product IFU and practitioner judgement; massage and aftercare per clinician protocol.
  • Inspect product packaging for integrity prior to use and follow local sharps disposal and handling regulations.

Contraindications

  • Not publicly listed

Adverse Effects

  • Not publicly listed

Storage Conditions

  • Manufacturer/distributor product literature and listings reference standard storage: keep in original packaging, protect from extreme temperatures and direct sunlight; consult product labelling/IFU for exact storage temperature range.

Duration

Not publicly listed

Onset

Not publicly listed

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