FDA UDI In Commercial Distribution 🇺🇸 United States

CryoPro mini

DI: 05710188020022 · Model: 19 · Cortex Technology ApS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
CryoPro mini
Primary DI
05710188020022
Version / Model
19
Catalog Number
E0200219
Company Name
Cortex Technology ApS
Labeler DUNS
306186800
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-26
Public Version
4
Public Version Date
2021-04-07
Public Version Status
Update
Public Device Record Key
3b6de475-0626-43b3-8d3b-a542da493908

Device Description

Cryosurgical equipment with accessories

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
No
Has Manufacturing Date
No
Has Expiration Date
No
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 05710188020022

Customer Contacts

Phone
+4598574100

Premarket Submissions

Submission Number Supplement Number
K982280 000