DI2315
Part of a family of 115 devices: see the family page
Ref DI2315
DI2315 is a Class I device made by ZimVie US Corp LLC, registered in EUDAMED on 29 May 2026 (Basic UDI-DI 844868A2GU) and listed in FDA GUDID since 4 Jan 2018 (UDI-DI 00844868002130), 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 | Number844868A2GU 00844868002130 | Date29 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00844868002130 | Date4 Jan 2018 | StatusListed |
Official records
- EUDAMED public site 844868A2GU
- AccessGUDID record 00844868002130
Across registries
- EUDAMED Basic UDI-DI 844868A2GU registered 29 May 2026 Active
- FDA GUDID UDI-DI 00844868002130 listed 4 Jan 2018 Listed
Timeline
- Listed FDA GUDID 00844868002130
- Registered EUDAMED 844868A2GU
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Dental implantation depth/angle gauge, reusable
- Device name
- Non-Sterile Manual Dental Instruments
- Model / reference
- DI2315
- Primary DI / UDI-DI
- 00844868002130
- Basic UDI-DI
- 844868A2GU
- FDA product code
- NDP
- EMDN code
- Q0199 Odontology devices - other
- GMDN term
- Dental implantation depth/angle gauge, reusable
- Device class
- Class I
- Regulation number
- 872.3980
- EU registration type
- Standard device
- EU market of registration
- Spain
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 15 Millimeter
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