← Back to catalogue

Esmarch Bandage Length: 500 cm +1 more model

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 20-20-100

by VBM Medizintechnik GmbH

Identity

Trade Name
Esmarch Bandage Length: 500 cm; 10 cm EUDAMED
n.a. FDA UDI
Generic Name
Pressure bandage, non-latex, reusable FDA UDI
Device Name
Tourniquet Consumables - Esmarch Bandage non-sterile EUDAMED
Esmarch Bandage FDA UDI
Model / Reference
20-20-100 EUDAMEDFDA UDI
Description
Esmarch Bandage FDA UDI

Identifiers

Primary DI / UDI-DI
04250105605693 EUDAMEDFDA UDI
Basic UDI-DI
42501056-3.3.1-n-NU EUDAMED
FDA Product Code
FQM FDA UDI
EMDN Code
Z12139006 PNEUMATIC TOURNIQUETS EUDAMED
GMDN Term
Pressure bandage, non-latex, reusable FDA UDI
Models / Variants
10 cm EUDAMEDFDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5075 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 — 500 Centimeter FDA UDI
Width — 10 Centimeter FDA UDI

Category: Tourniquet cuff, single-use

Esmarch Bandage Length: 500 cm +1 more model 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 762d6361-0b85-45d6-9d12-62ec56cc0a38 61 fields · synced Jun 18, 2026
  • FDA UDI 5ba63444-1ffd-481a-aca6-2670e0d399bf 36 fields · synced May 30, 2026