Silicone Double Cuff for leg

FDA UDI

Class I (US FDA UDI)

by VBM Medizintechnik GmbH

Identity

Trade Name: Silicone Double Cuff for leg FDA UDI
Generic Name: Tourniquet cuff, reusable FDA UDI
Device Name: Length: 61 cm / 24 inch FDA UDI
Model / Reference: 20-60-722 FDA UDI
Description: Length: 61 cm / 24 inch FDA UDI

Identifiers

Primary DI / UDI-DI: 04250105606942 FDA UDI
FDA Product Code: KCY FDA UDI
GMDN Term: Tourniquet cuff, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.5910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

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

Category: Tourniquet cuff, reusable

Silicone Double Cuff for leg by VBM Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, reusable.

Color Cuff — Stryker Corp. · Class I
Vari-Fit Reusable — Delfi Medical Innovations Inc · Class I
Reusable Conical Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
Easi-Fit BFR, Reusable — Delfi Medical Innovations Inc · Class I
Reusable Tourniquet Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
Reusable Tourniquet Cuff — Zhejiang Longyou Lande Medical Technology Co., Ltd. · Class I
ASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORP. · Class I
Vari-Fit Reusable — Delfi Medical Innovations Inc · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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

Manufacturer

Manufacturer: VBM Medizintechnik GmbH

Sources (1)

FDA UDI 95239c78-daf8-4624-b1e9-d081f3167f1e 36 fields · synced Jun 8, 2026