FDA UDI In Commercial Distribution 🇺🇸 United States

Cumulus Remover

DI: 04582231461202 · Model: Cumulus Remover · KITAZATO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Cumulus Remover
Primary DI
04582231461202
Version / Model
Cumulus Remover
Catalog Number
94111
Company Name
KITAZATO CORPORATION
Labeler DUNS
711091157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-25
Public Version
3
Public Version Date
2023-08-21
Public Version Status
Update
Public Device Record Key
26554dd4-bc82-48bf-903f-4ce897c5b2de

Device Description

1 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
No
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
44046 IVF medium

Identifiers

Type ID
Package 14582231461209
Primary 04582231461202

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 8 Degrees Celsius