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Tourniquet Wipe Cuff, Single Cuff 35 cm / 14 inch

by VBM Medizintechnik GmbH

Ref 20-75-711

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42501056-3.2.8-WD Basic UDI-DI 14250105628996UDI-DIDate9 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14250105628996 UDI-DI Date11 Aug 2023ListedStatusListed 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  • Withdrawn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
Tourniquet Wipe Cuff, Single Cuff 35 cm / 14 inch EUDAMED
Tourniquet Wipe Cuff, Single Cuff GUDID
Generic Name
Tourniquet cuff, reusable
Device Name
Tourniquet Cuffs - Wipe Cuff
Model / Reference
20-75-711
Primary DI / UDI-DI
14250105628996
Basic UDI-DI
42501056-3.2.8-WD
Direct Marketing DI
04250105628999
FDA Product Code
KCY
EMDN Code
Z12139006 Pneumatic tourniquets
GMDN Term
Tourniquet cuff, reusable
Device Class
Class I
Regulation Number
878.5910
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Length — 14 Inch
Length — 35 Centimeter

Manufacturer details

EUDAMED SRN
DE-MF-000005907

Other devices from VBM Medizintechnik GmbH

See all devices from VBM Medizintechnik GmbH →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: 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
  • Serial Number: No
  • Manufacturing Date: No