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BD Vacutainer® Stretch Latex Free Tourniquet

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® Stretch Latex Free Tourniquet FDA UDI
Generic Name
Venous tourniquet, single-use FDA UDI
Device Name
TOURNIQUET STRETCH LATEX FREE FDA UDI
Model / Reference
367203 FDA UDI
Description
TOURNIQUET STRETCH LATEX FREE FDA UDI

Identifiers

Catalog Number
367203 FDA UDI
Primary DI / UDI-DI
30382903672036 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 17.00 Inch FDA UDI

Category: Venous tourniquet, single-use

BD Vacutainer® Stretch Latex Free Tourniquet by Becton Dickinson And Company — 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

Sources (1)

  • FDA UDI 0a92933f-d4d6-45b3-906b-1abff247ba7a 36 fields · synced May 30, 2026