FDA UDI In Commercial Distribution 🇺🇸 United States

ReproPlate

DI: 04582231462704 · Model: ReproPlate-K1 · KITAZATO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReproPlate
Primary DI
04582231462704
Version / Model
ReproPlate-K1
Catalog Number
83007
Company Name
KITAZATO CORPORATION
Labeler DUNS
711091157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-01
Public Version
5
Public Version Date
2023-05-31
Public Version Status
Update
Public Device Record Key
3e2ceedb-da6b-4183-9da4-d28fe3634add

Device Description

Cell strage or handling

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
Yes
Has Serial Number
No
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
PUD Labware, assisted reproduction, exempt

GMDN Terms

Code Name
56648 Assisted reproduction procedure dish

Identifiers

Type ID
Primary 04582231462704