FDA UDI In Commercial Distribution 🇺🇸 United States

ReproPlate-K1(6Well)

DI: 04582231462391 · Model: ReproPlate-K1(6Well) · KITAZATO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ReproPlate-K1(6Well)
Primary DI
04582231462391
Version / Model
ReproPlate-K1(6Well)
Catalog Number
83006
Company Name
KITAZATO CORPORATION
Labeler DUNS
711091157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-18
Public Version
2
Public Version Date
2023-05-31
Public Version Status
Update
Public Device Record Key
60c66a59-d997-4710-8590-e42d603f5168

Device Description

10 Packs

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
MQL MEDIA, REPRODUCTIVE

GMDN Terms

Code Name
42850 IVF medium kit

Identifiers

Type ID
Primary 04582231462391

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius