7305781
Ref 7305.781Model 10000201541
7305781 (7305.781) is a device classified as Class IIa in the EU and Class II in the US made by Richard Wolf GmbH, registered in EUDAMED on 3 Sep 2026 (Basic UDI-DI B-04055207013670) and listed in FDA GUDID since 29 Sep 2016 (UDI-DI 04055207013670), 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-04055207013670 04055207013670 | Date3 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207013670 | Date29 Sep 2016 | StatusListed |
Official records
- EUDAMED public site B-04055207013670
- AccessGUDID record 04055207013670
Across registries
- EUDAMED Basic UDI-DI B-04055207013670 registered 3 Sep 2026 Active
- FDA GUDID UDI-DI 04055207013670 listed 29 Sep 2016 Listed
Timeline
- Listed FDA GUDID 04055207013670
- Registered EUDAMED B-04055207013670
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Pin-indexed adaptor, reusable
- Device name
- Adapters
- Model / Ref / Catalog
- 10000201541, 7305.781, 7305781
- Description
- ADAPTER TL 36mm, with 2 Luer connections, male, quick-lock, reusable
- Primary DI / UDI-DI
- 04055207013670
- Basic UDI-DI
- B-04055207013670
- FDA product code
- FAJ
- EMDN code
- A070199 Adapters and connectors - other
- GMDN term
- Pin-indexed adaptor, reusable
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 876.1500
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000201541 7305.781 | 7305781 |
| Device class | Class IIa | Class II |
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