devemed 110
by devemed GmbH
Part of a family of 43 devices: see the family page
Ref 110
devemed 110 is a dental impression tray (EU MDR Class I; FDA Class I; FDA product code EHY, Tray, Impression, Preformed) made by devemed GmbH, registered in EUDAMED on 14 Jul 2026 (Basic UDI-DI 4061644PG1104CJ) and listed in FDA GUDID since 28 Apr 2020 (UDI-DI 04061644005741), active as of 24 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number4061644PG1104CJ 04061644005741 | Date14 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04061644005741 | Date28 Apr 2020 | StatusListed |
Official records
- EUDAMED public site 4061644PG1104CJ
- AccessGUDID record 04061644005741
Across registries
- EUDAMED Basic UDI-DI 4061644PG1104CJ registered 14 Jul 2026 Active
- FDA GUDID UDI-DI 04061644005741 listed 28 Apr 2020 Listed
Timeline
- Listed FDA GUDID 04061644005741
- Registered EUDAMED 4061644PG1104CJ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- devemed
- Generic name
- Dental impression tray, reusable
- Device name
- Impression Trays
- Model / reference
- 110
- Primary DI / UDI-DI
- 04061644005741
- Basic UDI-DI
- 4061644PG1104CJ
- Direct marketing DI
- 04061644005741
- FDA product code
- EHY
- EMDN code
- Q010207 Dental impression devices for prosthetic dentistry
- GMDN term
- Dental impression tray, reusable
- Device class
- Class I
- Regulation number
- 872.6880
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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- Intraoral Scanner / by LargeV Instrument Corp., Ltd.
- Implant Replica Trefoil™ Conical Connection RP 38360 by Nobel Biocare AB
- Lilivis Y4XXCL-24-00001 by Huvitz Co., Ltd.