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IceSeed® 1.5 90° Cryoablation Needle

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
IceSeed® 1.5 90° Cryoablation Needle FDA UDI
Generic Name
Cryosurgical set FDA UDI
Device Name
1.5mm 90 degree Cryoablation Needle FDA UDI
Model / Reference
FPRPR3202 FDA UDI
Description
1.5mm 90 degree Cryoablation Needle FDA UDI

Identifiers

Catalog Number
FPRPR3202 FDA UDI
Primary DI / UDI-DI
07290104830235 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
MRI Safety
MR Unsafe FDA UDI

Category: Cryosurgical set

IceSeed® 1.5 90° Cryoablation Needle by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryosurgical set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 7ce6ca12-0659-47cd-bfbf-f59f74b95d06 37 fields · synced Jun 1, 2026