← 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
Laparoscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
STERILE LAVH PACK FDA UDI
Model / Reference
SMA43LAWKG FDA UDI
Description
STERILE LAVH PACK FDA UDI

Identifiers

Catalog Number
SMA43LAWKG FDA UDI
Primary DI / UDI-DI
10887488889566 FDA UDI
FDA Product Code
OJF FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, single-use 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: Laparoscopic surgical procedure kit, non-medicated, single-use

Cardinal Health's STERILE LAVH PACK is a sterile laparoscopic surgical procedure kit designed for non-medicated single-use hysterectomy procedures. This device meets the requirements of FDA regulations, ensuring compliance and quality in medical devices.

Similar devices

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

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 2df112a6-db28-44b5-b1ba-c89a967b3f73 34 fields · synced Jul 22, 2026