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Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Pelvic examination kit FDA UDI
Device Name
ANTERIOR PELVIC REPAIR PACK FDA UDI
Model / Reference
SMAHFAPNUC FDA UDI
Description
ANTERIOR PELVIC REPAIR PACK FDA UDI

Identifiers

Catalog Number
SMAHFAPNUC FDA UDI
Primary DI / UDI-DI
10197106641224 FDA UDI
FDA Product Code
MLT FDA UDI
GMDN Term
Pelvic examination kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 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: Pelvic examination kit

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

Similar devices

Also classified as Pelvic examination kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 3cacdbb7-d3d2-4a93-a3f6-ff52e139b669 35 fields · synced Jun 8, 2026