B.braun 8713112D
Part of a family of 10 devices: see the family page
Ref 8713112D
B.braun 8713112D is a device classified as Class I in the EU and Class II in the US made by B. Braun Medical, Inc., registered in EUDAMED on 29 Jul 2026 (Basic UDI-DI 403923900000024825) and listed in FDA GUDID since 27 Apr 2020 (UDI-DI 04046964085673), active as of 25 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number403923900000024825 04046964085673 | Date29 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04046964085673 | Date27 Apr 2020 | StatusListed |
Official records
- EUDAMED public site 403923900000024825
- AccessGUDID record 04046964085673
Across registries
- EUDAMED Basic UDI-DI 403923900000024825 registered 29 Jul 2026 Active
- FDA GUDID UDI-DI 04046964085673 listed 27 Apr 2020 Listed
Timeline
- Listed FDA GUDID 04046964085673
- Registered EUDAMED 403923900000024825
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Power supply SP EUDAMEDB.braun GUDID
- Generic name
- Basic power supply, reusable
- Device name
- Acc Space_power supply
- Model / Ref / Catalog
- 8713112D
- Primary DI / UDI-DI
- 04046964085673
- Basic UDI-DI
- 403923900000024825
- Direct marketing DI
- 04046964085673
- FDA product code
- FRN, LZH
- EMDN code
- Z12030380 Infusion instruments - hardware accessories
- GMDN term
- Basic power supply, reusable
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 880.5725
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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