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Tourniquet Wipe Cuff, Single Cuff 76 cm / 30 inch

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20-78-727Ref 20-75-727

by VBM Medizintechnik GmbH

Identity

Trade Name
Tourniquet Wipe Cuff, Single Cuff 76 cm / 30 inch EUDAMED
Tourniquet Wipe Cuff, Single Cuff FDA UDI
Generic Name
Tourniquet cuff, reusable FDA UDI
Device Name
Tourniquet Cuffs - Wipe Cuff EUDAMED
76 cm / 30 inch FDA UDI
Model / Reference
20-78-727 EUDAMED
20-75-727 EUDAMEDFDA UDI
Description
76 cm / 30 inch FDA UDI

Identifiers

Primary DI / UDI-DI
14250105629085 EUDAMED
14250105629078 EUDAMEDFDA UDI
Basic UDI-DI
42501056-3.2.8-WD EUDAMED
Direct Marketing DI
04250105629088 EUDAMED
04250105629071 EUDAMED
FDA Product Code
KCY FDA UDI
EMDN Code
Z12139006 PNEUMATIC TOURNIQUETS EUDAMED
GMDN Term
Tourniquet cuff, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.5910 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 24 Inch FDA UDI
Length — 61 Centimeter FDA UDI

Category: Tourniquet cuff, single-use

Tourniquet Wipe Cuff, Single Cuff 76 cm / 30 inch by VBM Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Tourniquet cuff, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005907

Sources (3)

  • EUDAMED 1c9c64a4-94df-409f-a280-59179beaa69d 61 fields · synced Jul 22, 2026
  • EUDAMED 9d846385-c05a-4052-aa44-f5c48cdeebda 61 fields · synced May 17, 2026
  • FDA UDI 96a766df-2c91-4af8-b37f-4a72593d28f7 36 fields · synced May 29, 2026