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Volvo 32367462

by DC Safety Sales

Ref 32394324

Volvo 32367462 (32394324) is a device classified as Class I (EU), Not classified (US) made by DC Safety Sales, registered in EUDAMED on 15 May 2026 (Basic UDI-DI 00816058012465DQ) and listed in FDA GUDID since 7 Oct 2022 (UDI-DI 00816058012465), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number00816058012465DQ Basic UDI-DI 00816058012465UDI-DIDate15 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00816058012465 UDI-DI Date7 Oct 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 00816058012465DQ registered 15 May 2026 Active
  • FDA GUDID UDI-DI 00816058012465 listed 7 Oct 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00816058012465
  2. Registered EUDAMED 00816058012465DQ

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  • Withdrawn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
Volvo
Generic name
Medical bag
Device name
Din 13164
Model / Ref / Catalog
32394324, 32367462
Description
First Aid Kit DIN
Primary DI / UDI-DI
00816058012465
Basic UDI-DI
00816058012465DQ
FDA product code
LRR
EMDN code
T0203 Dressing and assistance kits
GMDN term
Medical bag
Device class
Class I EUDAMED
N GUDID
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
First Aid Kit/DIN 13164
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
32394324
GUDID
32367462
Device classEUDAMED
Class I
GUDID
N
Supplied sterileEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Supplied sterile UDI-DI 00816058012465: EUDAMED states Yes, FDA GUDID states No.

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

Related devices

Category: Medical bag

Similar devices in this category

Other devices filed under DRESSING AND ASSISTANCE KITS.

Other devices from DC Safety Sales

See all devices from DC Safety Sales →

Properties

  • Supplied sterile YesEUDAMEDNoGUDID
  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
Other properties (10, all answered No)