Identity
- Trade Name
- Controller, Full/Swipe FDA UDI
- Generic Name
- High-pressure medical gas hose FDA UDI
- Device Name
- Controller for Full and Swipe C2 CryoBalloon Ablation System (translating) FDA UDI
- Model / Reference
- FG-1006 FDA UDI
- Description
- Controller for Full and Swipe C2 CryoBalloon Ablation System (translating) FDA UDI
Identifiers
- Catalog Number
- FG-1006 FDA UDI
- Primary DI / UDI-DI
- 00854924006064 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- High-pressure medical gas hose 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
No
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-medicatedHigh-pressure medical gas hose
Controller, Full/Swipe by C2 Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- C2 Therapeutics, Inc.
Sources (1)
- FDA UDI e5f5e2cb-a6a6-4460-86d2-56dd0eee4cd5 35 fields · synced Jun 1, 2026