Stoma® 7791.10
Part of a family of 85 devices: see the family page
Ref 7791.10Model 41660 - Periodontal curette (039)
Stoma® 7791.10 is a Class I device made by Storz am Mark GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI ++ESAM03997) and listed in FDA GUDID since 27 Aug 2020 (UDI-DI +ESAM7791101), active as of 23 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 | Number++ESAM03997 +ESAM7791101 | Date5 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number+ESAM7791101 | Date27 Aug 2020 | StatusListed |
Official records
- EUDAMED public site ++ESAM03997
Across registries
- EUDAMED Basic UDI-DI ++ESAM03997 registered 5 Oct 2026 Active
- FDA GUDID UDI-DI +ESAM7791101 listed 27 Aug 2020 Listed
Timeline
- Listed FDA GUDID +ESAM7791101
- Registered EUDAMED ++ESAM03997
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- color-stick Kürette, Barnhart B1-2, hellblau, Ø 10mm EUDAMEDStoma® GUDID
- Generic name
- Periodontal curette
- Model / Ref / Catalog
- 7791.10, 41660 - Periodontal curette (039)
- Primary DI / UDI-DI
- +ESAM7791101 EUDAMEDESAM7791101 GUDID
- Basic UDI-DI
- ++ESAM03997
- Direct marketing DI
- +ESAM7791100
- FDA product code
- EMS
- EMDN code
- L159099 Odontostomatology instruments, reusable - other
- GMDN term
- Periodontal curette
- Device class
- Class I
- Regulation number
- 872.4565
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Primary DI / UDI-DI | +ESAM7791101 | ESAM7791101 |
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