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Conmed

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Insufflation gas conditioning tubing set FDA UDI
Device Name
TUBING SET, WITH FILTER FOR LAPAROFLATOR FDA UDI
Model / Reference
C7011 FDA UDI
Description
TUBING SET, WITH FILTER FOR LAPAROFLATOR FDA UDI

Identifiers

Catalog Number
C7011 FDA UDI
Primary DI / UDI-DI
10845854080122 FDA UDI
FDA Product Code
NKC FDA UDI
GMDN Term
Insufflation gas conditioning tubing set 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

Yes

FDA UDI

Over-the-Counter

No

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: Insufflation gas conditioning tubing set

Conmed by Conmed Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insufflation gas conditioning tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 99e7c8a5-afaa-4934-90b9-185b6decb2ab 35 fields · synced May 29, 2026