Gimmi QS.1702.06
by Gimmi GmbH
Ref QS.1702.06
Gimmi QS.1702.06 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047081142) and listed in FDA GUDID since 22 May 2025 (UDI-DI 04049047081142), active as of 23 Oct 2026.
Active
CE MDD
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/MDD EUDAMED | NumberB-04049047081142 04049047081142 | Date8 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047081142 | Date22 May 2025 | StatusListed |
Official records
- EUDAMED public site B-04049047081142
- AccessGUDID record 04049047081142
Across registries
- EUDAMED Basic UDI-DI B-04049047081142 registered 8 Sep 2026 Active
- FDA GUDID UDI-DI 04049047081142 listed 22 May 2025 Listed
Timeline
- Listed FDA GUDID 04049047081142
- Registered EUDAMED B-04049047081142
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Gimmi
- Generic name
- ENT elevator
- Model / Ref / Catalog
- QS.1702.06
- Description
- FREER SEPTUM ELEVATOR SHARP/BLUNT, 6.5 MM LENGTH 195 MM
- Primary DI / UDI-DI
- 04049047081142
- Basic UDI-DI
- B-04049047081142
- FDA product code
- KAD
- EMDN code
- L149002 ENT levers, reusable
- GMDN term
- ENT elevator
- Device class
- Class I
- Regulation number
- 874.4420
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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