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Tourniquet Drape +1 more model

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 24-00-200-1

by VBM Medizintechnik GmbH

Identity

Trade Name
Tourniquet Drape; large ≥ 40 - 80 cm EUDAMED
Tourniquet Drape; large FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Device Name
Tourniquet Consumables - Drape sterile EUDAMED
40 - 80 cm FDA UDI
Model / Reference
24-00-200-1 EUDAMEDFDA UDI
Description
40 - 80 cm FDA UDI

Identifiers

Primary DI / UDI-DI
04250105630268 EUDAMEDFDA UDI
Basic UDI-DI
42501056-3.3.3-s-PR EUDAMED
FDA Product Code
KCY FDA UDI
EMDN Code
Z12139006 PNEUMATIC TOURNIQUETS EUDAMED
GMDN Term
Tourniquet cuff, single-use FDA UDI
Models / Variants
Tourniquet Drape EUDAMEDFDA UDI
large ≥ 40 - 80 cm 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

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Tourniquet cuff, single-use

Tourniquet Drape +1 more model by VBM Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — 2 models — regulatory data on deviCERTS

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

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Manufacturer

EUDAMED SRN
DE-MF-000005907

Sources (2)

  • EUDAMED f7f43254-1fbf-45ea-be04-35c3d25c44b2 61 fields · synced Sep 18, 2026
  • FDA UDI 94eab1b6-18c4-40f6-a5f3-62d955d59ce0 35 fields · synced May 30, 2026