# Acrifix 1351350

> Active: European Union and United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/acrifix-1351350>
- Manufacturer: [DeltaMed GmbH](https://devicerts.com/manufacturers/deltamed-gmbh) (Germany)
- Name in the registry: ACRIFIX 1351350
- Device class: Class IIa (EU MDR); Class II (US FDA)
- FDA product code: EBI, KLE
- EMDN: Q01020601 MOBILE DENTAL PROSTHESES
- EMDN: Q01020602 COMBINED DENTAL PROSTHESES
- EMDN: Q01020605 TEMPORARY DENTAL PROSTHESES
- GMDN: Dental prosthesis priming agent (62474)

## Registrations and authorizations

- **EUDAMED** · CE/MDR · European Union · Basic UDI-DI \++EDELTD05BUDI020009JA · UDI-DI \+EDEL13513500 · registered 2026-08-04 · status: Active
- **GUDID** · GUDID listing · United States · UDI-DI \+EDEL13513500 · listed 2023-05-12 · status: Listed (GUDID: in commercial distribution)
- **GUDID** · FDA 510(k) · United States · K212541 · decision 2022-01-10 · decision SESE · status: Active · from GUDID

## Recalls

No recall on record.

## Identity

- Trade name: ACRIFIX Bonder [EUDAMED]; ACRIFIX [FDA GUDID (AccessGUDID)]
- Generic name: Dental prosthesis priming agent [FDA GUDID (AccessGUDID)]
- Model / Ref / Catalog: 1351350 [EUDAMED, FDA GUDID (AccessGUDID)]; Denture Resins and Accessories - Bonding Resin for Denture Resins [EUDAMED]

## Identifiers

- Primary DI / UDI-DI: \+EDEL13513500 [EUDAMED]; EDEL13513500 [FDA GUDID (AccessGUDID)]
- Basic UDI-DI: \++EDELTD05BUDI020009JA [EUDAMED]
- 510(k) Number: K212541 [FDA GUDID (AccessGUDID)]
- FDA product code: EBI [FDA GUDID (AccessGUDID)]; KLE [FDA GUDID (AccessGUDID)]
- EMDN code: Q01020601 [EUDAMED]; Q01020602 [EUDAMED]; Q01020605 [EUDAMED]
- GMDN term: Dental prosthesis priming agent (62474) [FDA GUDID (AccessGUDID)]

## Classification

- Device class: Class IIa [EUDAMED]; Class II [FDA GUDID (AccessGUDID)]
- Regulation number: 872.3760 [FDA GUDID (AccessGUDID)]; 872.3200 [FDA GUDID (AccessGUDID)]
- EU registration type: Standard device [EUDAMED]
- EU market of registration: Germany [EUDAMED]
- GUDID distribution status: In Commercial Distribution [FDA GUDID (AccessGUDID)]

## Properties

- Single use: Yes [FDA GUDID (AccessGUDID)]
- Prescription use: Yes [FDA GUDID (AccessGUDID)]
- Lot / batch number: Yes [FDA GUDID (AccessGUDID)]
- Expiration date: Yes [FDA GUDID (AccessGUDID)]
- Supplied sterile: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Sterilise before use: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Implantable: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reusable: No [EUDAMED]
- Contains latex: No [EUDAMED, FDA GUDID (AccessGUDID)]
- Reprocessed single-use device: No [EUDAMED]
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No [EUDAMED]
- Incorporates a substance derived from human blood or plasma: No [EUDAMED]
- Contains human tissues or cells: No [EUDAMED]
- Contains animal tissues or cells: No [EUDAMED]
- Contains endocrine-disrupting substances: No [EUDAMED]
- Administering medicine: No [EUDAMED]
- Measuring function: No [EUDAMED]
- Incorporates a medicinal substance: No [EUDAMED]
- Over-the-counter: No [FDA GUDID (AccessGUDID)]
- Convenience kit: No [FDA GUDID (AccessGUDID)]
- Combination product: No [FDA GUDID (AccessGUDID)]
- HCT/P: No [FDA GUDID (AccessGUDID)]
- Premarket exempt: No [FDA GUDID (AccessGUDID)]
- Serial number: No [FDA GUDID (AccessGUDID)]
- Manufacturing date: No [FDA GUDID (AccessGUDID)]

## Source and citation

- Cite as: Acrifix 1351350, DeltaMed GmbH. deviCERTS medical device catalogue. https://devicerts.com/devices/acrifix-1351350 (data as of 2026-11-14).
- Data sources: [FDA GUDID (AccessGUDID)](https://accessgudid.nlm.nih.gov/), [EUDAMED](https://ec.europa.eu/tools/eudamed)
- Registry records last synced: 2026-10-24
- Statuses computed as of: 2026-11-14
- JSON: <https://devicerts.com/devices/acrifix-1351350.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/acrifix-1351350
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.