Amsco 5052
by Corporation Steris Canada 7 variants
Ref FH14072Model AMSCO 5052 Washer
Amsco 5052 (FH14072) is a device classified as Class IIa in the EU and Class II in the US made by Corporation Steris Canada, registered in EUDAMED on 25 Jun 2026 (Basic UDI-DI B-00724995192976) and listed in FDA GUDID since 4 Sep 2020 (UDI-DI 00724995192976), 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-00724995192976 00724995192976 | Date25 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00724995192976 | Date4 Sep 2020 | StatusListed |
Official records
- EUDAMED public site B-00724995192976
- AccessGUDID record 00724995192976
Across registries
- EUDAMED Basic UDI-DI B-00724995192976 registered 25 Jun 2026 Active
- FDA GUDID UDI-DI 00724995192976 listed 4 Sep 2020 Listed
Timeline
- Listed FDA GUDID 00724995192976
- Registered EUDAMED B-00724995192976
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Amsco
- Generic name
- Instrument non-thermal chemical disinfector
- Device name
- AMSCO 5052 Washer
- Model / Ref / Catalog
- AMSCO 5052 Washer, FH14072, 5052
- Primary DI / UDI-DI
- 00724995192976
- Basic UDI-DI
- B-00724995192976
- FDA product code
- MEC
- EMDN code
- Z12011311 Endoscope washers
- GMDN term
- Instrument non-thermal chemical disinfector
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 880.6992
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | AMSCO 5052 Washer FH14072 | 5052 |
| Device class | Class IIa | Class II |
Similar devices in this category
Other devices filed under ENDOSCOPE WASHERS.