← 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
Amniocentesis kit, non-medicated FDA UDI
Device Name
AMNIOCENTESIS TRAY FDA UDI
Model / Reference
SBA32ATSVA FDA UDI
Description
AMNIOCENTESIS TRAY FDA UDI

Identifiers

Catalog Number
SBA32ATSVA FDA UDI
Primary DI / UDI-DI
10885425145225 FDA UDI
FDA Product Code
HIO FDA UDI
GMDN Term
Amniocentesis kit, non-medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1550 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: Amniocentesis kit, non-medicated

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

Similar devices

Also classified as Amniocentesis kit, non-medicated.

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 92e809ad-8eb7-4df4-a8f4-89ebb722b3f4 34 fields · synced Jun 8, 2026