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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
Laparoscopic surgical procedure kit, medicated FDA UDI
Device Name
GENERAL LAPAROSCOPY PACK FDA UDI
Model / Reference
SBA23LAHM8 FDA UDI
Description
GENERAL LAPAROSCOPY PACK FDA UDI

Identifiers

Catalog Number
SBA23LAHM8 FDA UDI
Primary DI / UDI-DI
10197106785676 FDA UDI
FDA Product Code
FDE FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Laparoscopic surgical procedure kit, medicated

A comprehensive guide to the CARDINAL HEALTH Laparoscopic Surgical Procedure Kit, a single-use medical device for laparoscopy. This kit provides everything needed for a successful procedure, from sterile instruments to dressings and pharmaceuticals.

Similar devices

Also classified as Laparoscopic surgical procedure kit, medicated.

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 c0a6b104-d406-44b8-ba79-15ed8cba6128 35 fields · synced Oct 6, 2026