HipCheck

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: HipCheck FDA UDI
Generic Name: Portable active medical device mount FDA UDI
Model / Reference: 01030500 FDA UDI

Identifiers

Catalog Number: 0103-0500 FDA UDI
Primary DI / UDI-DI: 07613327424003 FDA UDI
FDA Product Code: FQO FDA UDI
GMDN Term: Portable active medical device mount FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4960 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Portable active medical device mount

HipCheck by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Stryker Corp.

Sources (1)

FDA UDI 28a88c07-7066-4cf4-8e4c-8ae393ef8ce9 34 fields · synced May 30, 2026