FDA UDI In Commercial Distribution 🇺🇸 United States

CryoIQ PRO liquid D2

DI: 07350006443015 · Model: CIQ-P-L/D2 · CryoIQ global AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CryoIQ PRO liquid D2
Primary DI
07350006443015
Version / Model
CIQ-P-L/D2
Catalog Number
CIQ-P-L/D2
Company Name
CryoIQ global AB
Labeler DUNS
632587858
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-16
Public Version
1
Public Version Date
2025-07-24
Public Version Status
New
Public Device Record Key
c5d9ed72-3822-4351-bb94-3d93375e1ec8

Device Description

CryoIQ PRO liquid/Derm 2

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEH Unit, Cryosurgical, Accessories

GMDN Terms

Code Name
11067 General cryosurgical system, cryogen gas, mechanical

Identifiers

Type ID
Primary 07350006443015

Premarket Submissions

Submission Number Supplement Number
K172049 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 122 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Protect from sunlight