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20-18-602

by VBM Medizintechnik GmbH

Ref 20-18-602

20-18-602 is a Class I device made by VBM Medizintechnik GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI 42501056-3.1.4-VS) and listed in FDA GUDID since 18 Sep 2020 (UDI-DI 14250105606529), 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 Number42501056-3.1.4-VS Basic UDI-DI 14250105606529UDI-DIDate30 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14250105606529 UDI-DI Date18 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42501056-3.1.4-VS registered 30 Mar 2026 Active
  • FDA GUDID UDI-DI 14250105606529 listed 18 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 14250105606529
  2. Registered EUDAMED 42501056-3.1.4-VS

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  • Withdrawn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
Manual Tourniquet 600 mmHg
Generic name
Surgical pneumatic tourniquet system
Device name
Tourniquet Devices - TQ-Manual
Model / reference
20-18-602
Primary DI / UDI-DI
14250105606529
Basic UDI-DI
42501056-3.1.4-VS
Direct marketing DI
04250105606522
FDA product code
KCY
EMDN code
Z12139006 Pneumatic tourniquets
GMDN term
Surgical pneumatic tourniquet system
Device class
Class I
Regulation number
878.5910
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical pneumatic tourniquet system

Similar devices in this category

Other devices filed under PNEUMATIC TOURNIQUETS.

Other devices from VBM Medizintechnik GmbH

See all devices from VBM Medizintechnik GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)