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C-Warmer Pink

by DXM Co., Ltd.

Ref CWB

C-Warmer Pink (CWB) is an anaesthesia warmer (EU MDR Class I; FDA Class I; FDA product code EFC, Warmer, Anesthetic Tube) made by Dxm Co., Ltd, registered in EUDAMED on 25 May 2025 (Basic UDI-DI 88000179WARMERPS) and listed in FDA GUDID since 19 Jun 2023 (UDI-DI 08800017900087), 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 Number88000179WARMERPS Basic UDI-DI 08800017900087UDI-DIDate25 May 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number08800017900087 UDI-DI Date19 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 88000179WARMERPS registered 25 May 2025 Active
  • FDA GUDID UDI-DI 08800017900087 listed 19 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08800017900087
  2. Registered EUDAMED 88000179WARMERPS

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  • Withdrawn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
C-Warmer Pink EUDAMED
C-Warmer GUDID
Generic name
Anaesthesia warmer
Model / Ref / Catalog
CWB EUDAMED
Pink GUDID
Primary DI / UDI-DI
08800017900087
Basic UDI-DI
88000179WARMERPS
Direct marketing DI
08800017900087
FDA product code
EFC
EMDN code
Z12019099 Various instruments for general and multidisciplinary surgery - other
GMDN term
Anaesthesia warmer
Device class
Class I
Regulation number
872.6100
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
CWB
GUDID
Pink

Manufacturer details

EUDAMED SRN
KR-MF-000016586
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - OTHER.

Other devices from Dxm Co., Ltd

See all devices from Dxm Co., Ltd →

Properties

  • Reusable
  • Serial number
Other properties (23, all answered No)