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CryoIQ Dermatology tip D1

FDA UDI

Class II (US FDA UDI)

by CryoIQ global AB

Identity

Trade Name
CryoIQ Dermatology tip D1 FDA UDI
Generic Name
General cryosurgical system, cryogen gas, mechanical FDA UDI
Device Name
Dermatology tip, L=22 mm, spray freezing Ø1-6 mm for PRO FDA UDI
Model / Reference
CIQ-PA-D1 FDA UDI
Description
Dermatology tip, L=22 mm, spray freezing Ø1-6 mm for PRO FDA UDI

Identifiers

Catalog Number
CIQ-PA-D1 FDA UDI
Primary DI / UDI-DI
07350006443596 FDA UDI
510(k) Number
K172049 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General cryosurgical system, cryogen gas, mechanical

CryoIQ Dermatology tip D1 by CryoIQ global AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General cryosurgical system, cryogen gas, mechanical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CryoIQ global AB

Sources (1)

  • FDA UDI a348f62d-c3c7-4107-8eeb-cd1803674659 35 fields · synced May 30, 2026