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Frigitronics

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
Frigitronics FDA UDI
Generic Name
Cryogenic analgesia unit FDA UDI
Device Name
Cryoanalgesia, 19 gauge Trocar Tip Probe. Tip: 1.0mm length x 1.0mm diameter. Shaft: 100mm length x 1.0mm diameter. FDA UDI
Model / Reference
239 FDA UDI
Description
Cryoanalgesia, 19 gauge Trocar Tip Probe. Tip: 1.0mm length x 1.0mm diameter. Shaft: 100mm length x 1.0mm diameter. FDA UDI

Identifiers

Primary DI / UDI-DI
00888937004281 FDA UDI
FDA Product Code
HQA FDA UDI
GMDN Term
Cryogenic analgesia unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4170 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cryogenic analgesia unit

Frigitronics by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryogenic analgesia unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CooperSurgical, Inc.

Sources (1)

  • FDA UDI c248fda5-3f74-43c0-9d52-f47f380f524c 33 fields · synced Jun 9, 2026