ChondroFiller®liquidPatient and professional information

Medical device information

Medical device information for ChondroFiller.

The manufacturer, register status, conformity, intended purpose, formats and vigilance route for ChondroFiller® liquid.

ChondroFiller liquid 2.3 ml pack with the dual-chamber syringe in its sterile blister

Manufacturer

Manufactured by Meidrix Biomedicals GmbH.

ChondroFiller is manufactured by Meidrix Biomedicals GmbH, Esslingen, Germany.

Register status

Listed on the MHRA register.

The manufacturer is listed on the MHRA register of medical devices. Registration is not approval.

Conformity

CE marked by the manufacturer.

CE marked by the manufacturer; accepted on the Great Britain market under the current transitional arrangements for CE-marked devices. Current instructions for use remain authoritative.

The product label carries the CE mark with notified body number 0483.

Intended purpose

As stated by the manufacturer.

The manufacturer's patient information states: ‘The application is intended to be used for filling clearly delimited cartilage damage up to grade IV in joints such as the knee, hip, shoulder and ankle as well as in partial cartilage injuries, subchondral and osteochondral defects. The implant offers the patient's own cells the opportunity to migrate into the matrix for the associated tissue regeneration. At the same time it serves as protection against further cartilage degeneration. Use in other parts of the body, such as auricle or breast, is not permitted.’

Formats

Available pack sizes.

ChondroFiller formats, presentation and setting time.
PropertyValue
Formats1.0 ml, 1.5 ml, 2.3 ml
PresentationSupplied as a ready-to-use dual-chamber syringe: a collagen solution and a neutralising solution mixed through an adapter at the point of application.
Setting timeThe mixed matrix hardens into a hydrogel in approximately 3 to 5 minutes, per the manufacturer.

Information on this site

Two sections, written for two audiences.

The patient section of this site gives general information for patients and carers. It is not clinical advice and does not replace an assessment by a clinician.

The professional section is written for UK healthcare professionals and covers composition, indications, contraindications, handling, technique and evidence. Current instructions for use remain authoritative.

Date of preparation: September 2026.