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Hcs

FDA UDI

Class I (US FDA UDI)

by Dyad Medical Sourcing, Llc

Identity

Trade Name
HCS FDA UDI
Generic Name
Limb tourniquet, manual, single-use FDA UDI
Device Name
1” x 18” Tourniquet, Rolled/Perforated, Textured, Latex Free, Blue FDA UDI
Model / Reference
HCS5004 FDA UDI
Description
1” x 18” Tourniquet, Rolled/Perforated, Textured, Latex Free, Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00849027000538 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Limb tourniquet, manual, single-use

Hcs by Dyad Medical Sourcing, Llc — 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

Sources (1)

  • FDA UDI 5b79a065-30ed-47cc-92c0-375d831bfc57 33 fields · synced Jun 1, 2026