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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
Cardiothoracic surgical procedure kit, medicated, single-use FDA UDI
Device Name
ANGIOGRAPHY DRAPE PACK FDA UDI
Model / Reference
SANOCADPBC FDA UDI
Description
ANGIOGRAPHY DRAPE PACK FDA UDI

Identifiers

Catalog Number
SANOCADPBC FDA UDI
Primary DI / UDI-DI
10198956062122 FDA UDI
FDA Product Code
OEQ FDA UDI
GMDN Term
Cardiothoracic surgical procedure kit, medicated, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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: Cardiothoracic surgical procedure kit, medicated, single-use

A comprehensive medical device directory, providing detailed information on the Cardiothoracic Surgical Procedure Kit (Cardinal Health SANOCADPBC) including its features, usage, and regulatory compliance.

Similar devices

Also classified as Cardiothoracic surgical procedure kit, medicated, single-use.

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 941bfcf1-c6a7-40fd-a4fe-9b93fd87ec64 35 fields · synced Oct 7, 2026