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VACSURE Disposable Tourniquets

FDA UDI

Class I (US FDA UDI)

by Labotek Group Corp

Identity

Trade Name
VACSURE Disposable Tourniquets FDA UDI
Generic Name
Venous tourniquet, single-use FDA UDI
Device Name
VACSURE Disposable Tourniquets, TPE Material, 1" x 18" Pre-Notched FDA UDI
Model / Reference
VS-DTD FDA UDI
Description
VACSURE Disposable Tourniquets, TPE Material, 1" x 18" Pre-Notched FDA UDI

Identifiers

Primary DI / UDI-DI
00850014448332 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Venous tourniquet, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Venous tourniquet, single-use

VACSURE Disposable Tourniquets by Labotek Group Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Venous tourniquet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Labotek Group Corp

Sources (1)

  • FDA UDI 2d745c33-3fb2-4977-96a0-48dd110724c4 35 fields · synced May 30, 2026