Identity
- Trade Name
- truFreeze FDA UDI
- Generic Name
- General cryosurgical system, cryogen gas, mechanical FDA UDI
- Device Name
- 20 FR CryoDecompression Tube (CDT) Active Venting is used with the truFreeze Spray Cryotherapy System. FDA UDI
- Model / Reference
- ACCCC3CDT05 FDA UDI
- Description
- 20 FR CryoDecompression Tube (CDT) Active Venting is used with the truFreeze Spray Cryotherapy System. FDA UDI
Identifiers
- Catalog Number
- ACCCC3CDT05 FDA UDI
- Primary DI / UDI-DI
- 00724995199203 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- General cryosurgical system, cryogen gas, mechanical 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
No
FDA UDI
Category: General cryosurgical system, cryogen gas, mechanical
truFreeze by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Cardioblate® CryoFlex® — MEDTRONIC, INC. · Class II
Cleared under the same submission
K171626 also covers:
K222272 also covers:
K223369 also covers:
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
- US Endoscopy
Sources (1)
- FDA UDI ebc78408-8117-4cb5-9064-392cbe59830a 37 fields · synced Jun 8, 2026