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Tourniquet Dispo Cuff - Double Cuff 30 cm / 12 inch

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20-30-710SLZ-1

by VBM Medizintechnik GmbH

Identity

Trade Name
Tourniquet Dispo Cuff; Double Cuff 30 cm / 12 inch EUDAMED
n.a. FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Device Name
Tourniquet Cuffs - Dispo Cuff EUDAMED
Double Cuff disposable for child FDA UDI
Model / Reference
20-30-710SLZ-1 EUDAMEDFDA UDI
Description
Double Cuff disposable for child FDA UDI

Identifiers

Primary DI / UDI-DI
04250105609844 EUDAMEDFDA UDI
Basic UDI-DI
42501056-3.2.1-VQ EUDAMED
FDA Product Code
KCY FDA UDI
EMDN Code
Z12139006 PNEUMATIC TOURNIQUETS EUDAMED
GMDN Term
Tourniquet cuff, single-use FDA UDI
Models / Variants
Tourniquet Dispo Cuff EUDAMEDFDA UDI
Double Cuff 30 cm / 12 inch EUDAMEDFDA 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

Yes

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 — 30 Centimeter FDA UDI

Category: Tourniquet cuff, single-use

Tourniquet Dispo Cuff - Double Cuff 30 cm / 12 inch by VBM Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — 2 models

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 (2)

  • EUDAMED bffc17f2-8c21-4827-80d9-86ce58286ac1 61 fields · synced Jun 18, 2026
  • FDA UDI aab34216-cc51-44d3-a1ef-8e75fc2df8db 36 fields · synced May 29, 2026