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Belotero® Revive

Belotero®

Belotero® Revive

Cross-linked hyaluronic acid with glycerol, without lidocaine. According to the manufacturer's instructions for use, it is indicated for revitalising prematurely sun-damaged skin of the cheeks, characterised by dehydration, loss of elasticity and firmness and superficial fine lines.

  • 20 mg/ml HA
  • 17.5 mg/ml glycerol
  • 1 × 1 ml

CE-marked medical device (CE 0123) · For trained healthcare professionals only

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  • Norwegian warehouse
  • 1 to 2 day delivery
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Description

What it is

Belotero Revive is an injectable, resorbable implant of cross-linked sodium hyaluronate of non-animal origin, with glycerol, produced with CPM technology. It is lidocaine-free.

Intended use (per instructions for use)

Intended to revitalise facial skin by rehydrating dry and very dry skin, increasing elasticity and firmness and smoothing superficial fine lines. Indicated for revitalising prematurely sun-damaged skin of the cheeks, characterised by dehydration, loss of elasticity and firmness and superficial fine lines. According to the manufacturer's clinical data, the product has been shown to last up to 9 months. The purpose of the product is purely aesthetic; no clinical benefits can be expected.

Composition

Sodium hyaluronate 20 mg/ml, glycerol 17.5 mg/ml, phosphate buffer pH 7 q.s. 1.0 ml. Residual BDDE ≤ 2 ppm.

Treatment

  • Contents: 1 pre-filled 1 ml syringe and 2 sterile single-use 30G½″ needles.
  • Injection: mid or deep dermis. The recommended technique is serial micropuncture with approximately 50 µl per point, 20–30 points approximately 1–2 cm apart. Inject slowly, aspirate before injecting and avoid overcorrection. See the instructions for use for maximum volume and interval.

Important to know

For injection only by healthcare professionals with training and knowledge of the anatomy. Contraindicated in case of known hypersensitivity to the constituents (including sodium hyaluronate, glycerol or BDDE), in pregnant or breastfeeding women, under 18 years of age, in case of general infection and in active autoimmune disease. Do not inject into blood vessels, into the glabella or nose area, into skin with active inflammation or infection, or into areas previously treated with a permanent skin filler. Rare but serious events have been reported after unintentional injection into facial blood vessels (including vision impairment, blindness, stroke and skin necrosis). Single-use device; do not re-sterilise or reuse.

Storage and shelf life

Store at 2–25 °C, protected from light and dry. Avoid mechanical shocks. Do not freeze. Check the packaging and expiry date before use.

Documentation and traceability

CE-marked (CE 0123). Manufacturer: Anteis SA, Plan-les-Ouates, Switzerland. Authorised representative in the EU: Merz Aesthetics GmbH, Frankfurt am Main, Germany. See the attached Norwegian instructions for use (version 4.0, 23.02.2026).

Ingredients and composition

Composition: sodium hyaluronate 20 mg/ml, glycerol 17.5 mg/ml, phosphate buffer pH 7 q.s. 1.0 ml. Residual BDDE ≤ 2 ppm. Lidocaine-free. 1 × 1 ml pre-filled syringe.

Directions and protocol

Inject into the mid or deep dermis of the cheeks. The recommended technique is serial micropuncture: several small injections evenly distributed across the treatment area, approximately 50 µl per point, 20–30 points approximately 1–2 cm apart. Inject slowly with the least possible pressure and use the enclosed needles (2 × 30G½″). Aspirate before injecting and avoid overcorrection. See the attached instructions for use for maximum volume and interval.

Specifications

Item no.:50114
Composition: Sodium hyaluronate 20 mg/ml, glycerol 17.5 mg/ml
Lidocaine: None (lidocaine-free)
Pack: 1 × 1 ml pre-filled syringe
Needles: ~7 (phosphate-citrate buffer)
Intended use: Revitalisation of prematurely sun-damaged skin of the cheeks
Storage: 2–25 °C, protected from light; do not freeze
Manufacturer: Anteis SA, Switzerland (EU rep. Merz Aesthetics GmbH)
Classification: CE-marked medical device (CE 0123)
Injection depth: Mid to deep dermis

Documentation and compliance

CE-marked medical device

LOT number and Declaration of Conformity accompany every shipment for your patient records.

The product information below is reserved for approved clinics. Log in

Shipping and returns

Ships from our Norwegian warehouse, typically 1 to 2 business days.

Sterile and lot-controlled goods cannot be returned for patient-safety reasons. Contact us for defects or transit damage.

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Frequently asked questions

What is the product?

Belotero Revive is an injectable, resorbable implant of cross-linked sodium hyaluronate (20 mg/ml) with glycerol (17.5 mg/ml), without lidocaine, supplied as 1 pre-filled 1 ml syringe.

What is the product intended for?

According to the instructions for use, it is indicated for revitalising prematurely sun-damaged skin of the cheeks, characterised by dehydration, loss of elasticity and firmness and superficial fine lines.

Which needles are included?

Two sterile single-use 30G½″ needles.

When must the product not be used?

Not in case of known hypersensitivity to the constituents (including sodium hyaluronate, glycerol or BDDE), in pregnant or breastfeeding women, under 18 years of age, in case of general infection or active autoimmune disease. Not into blood vessels, into the glabella or nose area, into skin with active inflammation or infection, or into areas previously treated with a permanent skin filler. See the instructions for use for the full list.

How is the product stored?

At 2–25 °C, protected from light. Do not freeze. The product is for single use.

Why BC Nordic

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CE marking, Declaration of Conformity and LOT numbers ready for your compliance archive.

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