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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
General specimen collection kit IVD, clinical FDA UDI
Device Name
Collection and Transport Swab Microorganism Collection and Transport System FDA UDI
Model / Reference
C8552-11S FDA UDI
Description
Collection and Transport Swab Microorganism Collection and Transport System FDA UDI

Identifiers

Catalog Number
C8552-11S FDA UDI
Primary DI / UDI-DI
10885380163517 FDA UDI
FDA Product Code
JSM FDA UDI
GMDN Term
General specimen collection kit IVD, clinical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2390 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen collection kit IVD, clinical

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

Similar devices

Also classified as General specimen collection kit IVD, clinical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e12c169d-2ba9-4139-97d4-86649f0538ea 35 fields · synced Jun 8, 2026