Stryker Tourniquet

FDA UDI

Class I (US FDA UDI)

by Renu Medical, Inc

Identity

Trade Name: Stryker Tourniquet FDA UDI
Generic Name: Surgical pneumatic tourniquet system FDA UDI
Device Name: Stryker Color Cuff II Adt 18x4in. 5921-218-235 FDA UDI
Model / Reference: RM-5921-218-235 FDA UDI
Description: Stryker Color Cuff II Adt 18x4in. 5921-218-235 FDA UDI

Identifiers

Primary DI / UDI-DI: 00816317023782 FDA UDI
FDA Product Code: KCY FDA UDI
GMDN Term: Surgical pneumatic tourniquet system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.5910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical pneumatic tourniquet system

Stryker Tourniquet by Renu Medical, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Surgical pneumatic tourniquet system.

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A.T.S.® Personalized Pressure® — Zimmer Orthopaedic Surgical Products · Class I
DTS-3000 — DAESUNG MAREF CO., LTD. · Class I
A.T.S.® Personalized Pressure® — Zimmer Orthopaedic Surgical Products · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Renu Medical, Inc

Sources (1)

FDA UDI ec091a6c-c56b-4600-a859-a9b6ab3ab36a 33 fields · synced May 30, 2026