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Marketlab

FDA UDI

Class I (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Marketlab FDA UDI
Generic Name
Limb tourniquet, manual, single-use FDA UDI
Device Name
Marketlab Latex-Free Tourniquets Bulk Pack, Pink PK1000; 1” Width, 18” Length, Pack of 1000 pcs. FDA UDI
Model / Reference
138029-PK FDA UDI
Description
Marketlab Latex-Free Tourniquets Bulk Pack, Pink PK1000; 1” Width, 18” Length, Pack of 1000 pcs. FDA UDI

Identifiers

Primary DI / UDI-DI
00817517027556 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Limb 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

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

Yes

FDA UDI

Category: Limb tourniquet, manual, single-use

Marketlab by Marketlab Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI b5494444-e151-4ace-8691-8b5c298c37b2 33 fields · synced May 31, 2026