← Back to catalogue

Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
KIT, TOTAL HIP HEMIARTHR, WAR FDA UDI
Model / Reference
POW1THWM9 FDA UDI
Description
KIT, TOTAL HIP HEMIARTHR, WAR FDA UDI

Identifiers

Catalog Number
POW1THWM9 FDA UDI
Primary DI / UDI-DI
10888439535280 FDA UDI
FDA Product Code
OJH FDA UDI
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, single-use

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 40ea0e36-7a6f-437c-9625-a7668f6ab9f9 34 fields · synced Jun 8, 2026