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20-64-528

by VBM Medizintechnik GmbH

20-64-528 is a Class I device made by VBM Medizintechnik GmbH, listed in FDA GUDID since 31 Aug 2020 (UDI-DI 04250105617641), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250105617641 UDI-DI Date31 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic name
Tourniquet cuff, reusable
Model / reference
20-64-528
Primary DI / UDI-DI
04250105617641
FDA product code
KCY
GMDN term
Tourniquet cuff, reusable
Device class
Class I
Regulation number
878.5910
GUDID distribution status
In Commercial Distribution
Size
Length — 86 Centimeter
Length — 34 Inch

Related devices

Category: Tourniquet cuff, reusable

Similar devices in this category

Other devices filed under Tourniquet cuff, reusable.

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)