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Dukal

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Dukal FDA UDI
Generic Name
Arterial tourniquet, manual, single-use FDA UDI
Device Name
Tourniquet, Non-Latex, 3/4" x 18", Blue FDA UDI
Model / Reference
4203 FDA UDI
Description
Tourniquet, Non-Latex, 3/4" x 18", Blue FDA UDI

Identifiers

Catalog Number
4203 FDA UDI
Primary DI / UDI-DI
10665973031641 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Arterial tourniquet, manual, 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arterial tourniquet, manual, single-use

Dukal by Dukal LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arterial tourniquet, manual, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dukal LLC

Sources (1)

  • FDA UDI 2a262eaa-39aa-429c-87a0-69d474fc280f 35 fields · synced Jun 6, 2026