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CryoIQ PRO liquid D2

FDA UDI

Class II (US FDA UDI)

by CryoIQ global AB

Identity

Trade Name
CryoIQ PRO liquid D2 FDA UDI
Generic Name
General cryosurgical system, cryogen gas, mechanical FDA UDI
Device Name
CryoIQ PRO liquid/Derm 2 FDA UDI
Model / Reference
CIQ-P-L/D2 FDA UDI
Description
CryoIQ PRO liquid/Derm 2 FDA UDI

Identifiers

Catalog Number
CIQ-P-L/D2 FDA UDI
Primary DI / UDI-DI
07350006443015 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 PRO liquid D2 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

K172049 also covers:

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 c5d9ed72-3822-4351-bb94-3d93375e1ec8 36 fields · synced May 30, 2026