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BD Angiocath IV Catheter 381123

by Becton, Dickinson and Company

Ref 381123

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number038290PLUSQXZORT Basic UDI-DIDate7 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00382903811236 UDI-DIDate16 Sep 2016ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Angiocath EUDAMED
BD Angiocath IV Catheter GUDID
Generic Name
Peripheral intravenous cannula
Device Name
BD Angiocath™ IV Catheter
Model / Ref / Catalog
381123
Primary DI / UDI-DI
00382903811236
Basic UDI-DI
038290PLUSQXZORT
FDA Product Code
FOZ
EMDN Code
C0101010102 Peripheral i.v. catheters, w/o safety systems, w/o injection valves
GMDN Term
Peripheral intravenous cannula
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
880.5200
Market of Registration
Poland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 25 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class II

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Properties

  • Sterile
  • Single Use
  • CMR Substance
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No