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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
Laparoscopic insufflator FDA UDI
Device Name
CARDINAL HEALTH INSUFFLATION TUBING 10 FT FDA UDI
Model / Reference
C-2000-ST FDA UDI
Description
CARDINAL HEALTH INSUFFLATION TUBING 10 FT FDA UDI

Identifiers

Catalog Number
C-2000-ST FDA UDI
Primary DI / UDI-DI
10885380144400 FDA UDI
FDA Product Code
NKC FDA UDI
GMDN Term
Laparoscopic insufflator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1730 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic insufflator

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

Similar devices

Also classified as Laparoscopic insufflator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d78249f7-860c-40d7-8366-3ad5363b0c77 34 fields · synced Jun 8, 2026