FDA UDI In Commercial Distribution 🇺🇸 United States

Unimax

DI: 04714127863573 · Model: FEP979000 · UNIMAX MEDICAL SYSTEMS INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Unimax
Primary DI
04714127863573
Version / Model
FEP979000
Company Name
UNIMAX MEDICAL SYSTEMS INC.
Labeler DUNS
658122465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-03
Public Version
1
Public Version Date
2022-05-11
Public Version Status
New
Public Device Record Key
1a70685f-65a7-427a-9b5d-ea8288cadce2

Device Description

Detachable endo pocket

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
45130 Tissue extraction bag

Identifiers

Type ID
Package 14714127863570
Primary 04714127863573
Package 24714127863577

Device Sizes

Type Value Unit Text
Width 3 Inch
Height 6 Inch