FDA UDI In Commercial Distribution 🇺🇸 United States

Cryotop US(R)

DI: 04582231462902 · Model: Cryotop US(R) · KITAZATO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cryotop US(R)
Primary DI
04582231462902
Version / Model
Cryotop US(R)
Catalog Number
81172
Company Name
KITAZATO CORPORATION
Labeler DUNS
711091157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-27
Public Version
3
Public Version Date
2023-05-31
Public Version Status
Update
Public Device Record Key
f1f3b17d-2a75-49d0-b823-308a67ec23c6

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MQK LABWARE, ASSISTED REPRODUCTION

GMDN Terms

Code Name
47446 Assisted reproduction vitrification carrier

Identifiers

Type ID
Package 14582231462909
Primary 04582231462902

Premarket Submissions

Submission Number Supplement Number
K153027 000