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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
Birthing/delivery kit FDA UDI
Device Name
HLTH FIRST VAGINAL DELIVERY PK FDA UDI
Model / Reference
SMA26VDHRR FDA UDI
Description
HLTH FIRST VAGINAL DELIVERY PK FDA UDI

Identifiers

Catalog Number
SMA26VDHRR FDA UDI
Primary DI / UDI-DI
10198956172708 FDA UDI
FDA Product Code
MLS FDA UDI
GMDN Term
Birthing/delivery 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: Birthing/delivery kit

A comprehensive medical device directory listing for the Cardinal Health Labor and Delivery Kit, providing detailed information on its features, compliance, and usage.

Similar devices

Also classified as Birthing/delivery 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 70c8cf8d-f4c6-4ef5-9b36-f8bd92b3808d 35 fields · synced Jul 8, 2026