← Back to catalogue

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
VAGINAL DELIVERY PACK FDA UDI
Model / Reference
SMA41VDT16 FDA UDI
Description
VAGINAL DELIVERY PACK FDA UDI

Identifiers

Catalog Number
SMA41VDT16 FDA UDI
Primary DI / UDI-DI
10888439656053 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

Cardinal Health's Labor and Delivery Kit (L&D) is a comprehensive, single-use device designed specifically for the birthing and delivery of newborns. This sterile kit contains all the necessary instruments, dressings, and pharmaceuticals required for this procedure, making it an ideal solution for healthcare professionals.

Similar devices

Also classified as Birthing/delivery kit.

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 def0400b-74ed-496c-bf8e-79c128b5176a 34 fields · synced Jun 22, 2026