LOCATOR R-Tx 30015-01
Ref 30015-01
LOCATOR R-Tx 30015-01 is a Class I device made by Zest Anchors, LLC, registered in EUDAMED on 9 Sep 2026 (Basic UDI-DI 08404811Z040EF) and listed in FDA GUDID since 6 Jul 2022 (UDI-DI 00840481110054), 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 | Number08404811Z040EF 00840481110054 | Date9 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840481110054 | Date6 Jul 2022 | StatusListed |
Official records
- EUDAMED public site 08404811Z040EF
- AccessGUDID record 00840481110054
Across registries
- EUDAMED Basic UDI-DI 08404811Z040EF registered 9 Sep 2026 Active
- FDA GUDID UDI-DI 00840481110054 listed 6 Jul 2022 Listed
Timeline
- Listed FDA GUDID 00840481110054
- Registered EUDAMED 08404811Z040EF
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- LOCATOR R-Tx
- Generic name
- Dental implant analog
- Device name
- Locator R-Tx Analog
- Model / reference
- 30015-01
- Primary DI / UDI-DI
- 00840481110054
- Basic UDI-DI
- 08404811Z040EF
- FDA product code
- NDP
- EMDN code
- P01020180 Dental implants - accessories
- GMDN term
- Dental implant analog
- Device class
- Class I
- Regulation number
- 872.3980
- 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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