Identity
- Trade Name
- IceSphere™ 1.5 CX Cryoablation Needle FDA UDI
- Generic Name
- Cryosurgical set FDA UDI
- Device Name
- 1.5 mm Cryoablation Needle FDA UDI
- Model / Reference
- FPRPR3573 FDA UDI
- Description
- 1.5 mm Cryoablation Needle FDA UDI
Identifiers
- Catalog Number
- FPRPR3573 FDA UDI
- Primary DI / UDI-DI
- 07290104831133 FDA UDI
- FDA Product Code
- GEH FDA UDI
- GMDN Term
- Cryosurgical set 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
MR Unsafe FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 1.5 Millimeter FDA UDIShaft Length — 175 Millimeter FDA UDI
Category: Cryosurgical set
IceSphere™ 1.5 CX Cryoablation Needle by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- RenalCryo™ — ENDOCARE, INC. · Class II
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- V2 ICE Probe SL — SANARUS TECHNOLOGIES, INC. · Class II
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
- Boston Scientific
Sources (1)
- FDA UDI 750ac15c-ae38-4b1c-9afa-6507a4b8943b 37 fields · synced May 30, 2026