Flexicare 030-620/1U
Ref 030-620/1U
Flexicare 030-620/1U is a device classified as Class IIa in the EU and Class I in the US made by Flexicare Medical Limited, registered in EUDAMED on 18 Aug 2026 (Basic UDI-DI B-05055788791317) and listed in FDA GUDID since 13 Mar 2024 (UDI-DI 05055788791317), active as of 25 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-05055788791317 05055788791317 | Date18 Aug 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05055788791317 | Date13 Mar 2024 | StatusListed |
Official records
- EUDAMED public site B-05055788791317
- AccessGUDID record 05055788791317
Across registries
- EUDAMED Basic UDI-DI B-05055788791317 registered 18 Aug 2026 Active
- FDA GUDID UDI-DI 05055788791317 listed 13 Mar 2024 Listed
Timeline
- Listed FDA GUDID 05055788791317
- Registered EUDAMED B-05055788791317
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Flexicare
- Generic name
- Y-piece breathing circuit connector, single-use
- Device name
- Breathing System Components and Accessories
- Model / reference
- 030-620/1U
- Primary DI / UDI-DI
- 05055788791317
- Basic UDI-DI
- B-05055788791317
- FDA product code
- BZA
- EMDN code
- R028099 Respiratory circuits and mount catheters - accessories not included in other classes
- GMDN term
- Y-piece breathing circuit connector, single-use
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 868.5810
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Northern Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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