S.7049.18
by Gimmi GmbH
Ref S.7049.18
S.7049.18 is a Class I device made by Gimmi GmbH, registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-04049047092247) and listed in FDA GUDID since 15 Jun 2023 (UDI-DI 04049047092247), 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-04049047092247 04049047092247 | Date8 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04049047092247 | Date15 Jun 2023 | StatusListed |
Official records
- EUDAMED public site B-04049047092247
- AccessGUDID record 04049047092247
Across registries
- EUDAMED Basic UDI-DI B-04049047092247 registered 8 Sep 2026 Active
- FDA GUDID UDI-DI 04049047092247 listed 15 Jun 2023 Listed
Timeline
- Listed FDA GUDID 04049047092247
- Registered EUDAMED B-04049047092247
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Flexible endoscopic scissors, reusable
- Model / reference
- S.7049.18
- Description
- SCISSORS SEMI-RIGID; Ø 1.6 MM / 5 CH; WORKING LENGTH 400 MM
- Primary DI / UDI-DI
- 04049047092247
- Basic UDI-DI
- B-04049047092247
- 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.