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B.braun 8713130

by B. Braun Medical, Inc.

Ref 8713130

B.braun 8713130 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 4039239000000226ZQ) and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04045928000202), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4039239000000226ZQ Basic UDI-DI 04045928000202UDI-DIDate29 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04045928000202 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000000226ZQ registered 29 Jul 2026 Active
  • FDA GUDID UDI-DI 04045928000202 listed 23 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04045928000202
  2. Registered EUDAMED 4039239000000226ZQ

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Pole clamp SP EUDAMED
B.braun GUDID
Generic name
Frame/rail/pole device holder
Device name
Acc Space_pole clamp
Model / Ref / Catalog
8713130
Primary DI / UDI-DI
04045928000202
Basic UDI-DI
4039239000000226ZQ
Direct marketing DI
04045928000202
FDA product code
FRN
EMDN code
Z12030380 Infusion instruments - hardware accessories
GMDN term
Frame/rail/pole device holder
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.5725
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Similar devices in this category

Other devices filed under INFUSION INSTRUMENTS - HARDWARE ACCESSORIES.

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Properties

  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (22, all answered No)