Olympus A2574
Ref A2574
Olympus A2574 is a flexible endoscopic tissue manipulation forceps (EU MDD Class I; FDA Class I; FDA product code KOA, Surgical Instruments, G-U, Manual (And Accessories)) made by Olympus Winter & Ibe GmbH, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-04042761003698) and listed in FDA GUDID since 27 Jan 2023 (UDI-DI 04042761003698), active as of 7 Nov 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-04042761003698 04042761003698 | Date6 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04042761003698 | Date27 Jan 2023 | StatusListed |
Official records
- EUDAMED public site B-04042761003698
- AccessGUDID record 04042761003698
Across registries
- EUDAMED Basic UDI-DI B-04042761003698 registered 6 Nov 2026 Active
- FDA GUDID UDI-DI 04042761003698 listed 27 Jan 2023 Listed
Timeline
- Listed FDA GUDID 04042761003698
- Registered EUDAMED B-04042761003698
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Grasping forceps, 5 Fr. x 600 mm EUDAMEDOlympus GUDID
- Generic name
- Flexible endoscopic tissue manipulation forceps, reusable
- Model / Ref / Catalog
- A2574
- Primary DI / UDI-DI
- 04042761003698
- Basic UDI-DI
- B-04042761003698
- FDA product code
- KOA
- EMDN code
- L060403 Endoscopic urology forceps, reusable
- GMDN term
- Flexible endoscopic tissue manipulation forceps, reusable
- Device class
- Class I
- Regulation number
- 876.4730
- 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 FORCEPS, REUSABLE.