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C2 CryoBalloon Swipe Catheter, Standard

FDA UDI

Class II (US FDA UDI)

by C2 Therapeutics, Inc.

Identity

Trade Name
C2 CryoBalloon Swipe Catheter, Standard FDA UDI
Generic Name
Gastrointestinal/biliary dilation balloon catheter, non-medicated FDA UDI
Device Name
C2 CryoBalloon Swipe Catheter with Standard Balloon for C2 CryoBalloon Ablation System FDA UDI
Model / Reference
FG-1015 FDA UDI
Description
C2 CryoBalloon Swipe Catheter with Standard Balloon for C2 CryoBalloon Ablation System FDA UDI

Identifiers

Catalog Number
FG-1015 FDA UDI
Primary DI / UDI-DI
00854924006156 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Gastrointestinal/biliary dilation balloon catheter, non-medicated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Gastrointestinal/biliary dilation balloon catheter, non-medicated

C2 CryoBalloon Swipe Catheter, Standard by C2 Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrointestinal/biliary dilation balloon catheter, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db7e2a44-08f7-4624-bcbf-1a205f12303c 35 fields · synced May 30, 2026