S.7052.24
by Gimmi GmbH
Ref S.7052.24
S.7052.24 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047092483) and listed in FDA GUDID since 15 Jun 2023 (UDI-DI 04049047092483), active as of 24 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-04049047092483 04049047092483 | Date8 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047092483 | Date15 Jun 2023 | StatusListed |
Official records
- EUDAMED public site B-04049047092483
- AccessGUDID record 04049047092483
Across registries
- EUDAMED Basic UDI-DI B-04049047092483 registered 8 Sep 2026 Active
- FDA GUDID UDI-DI 04049047092483 listed 15 Jun 2023 Listed
Timeline
- Listed FDA GUDID 04049047092483
- Registered EUDAMED B-04049047092483
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Flexible endoscopic scissors, reusable
- Model / reference
- S.7052.24
- Description
- SCISSORS SEMI-RIGID; Ø 2.3 MM / 7 CH, DOUBLE ACTION; WORKING LENGTH 400 MM
- Primary DI / UDI-DI
- 04049047092483
- Basic UDI-DI
- B-04049047092483
- FDA product code
- LRW
- EMDN code
- L060401 Endoscopic urology scissors, reusable
- GMDN term
- Flexible endoscopic scissors, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- 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
Similar devices in this category
Other devices filed under ENDOSCOPIC UROLOGY INSTRUMENTS, REUSABLE.