FDA UDI In Commercial Distribution 🇺🇸 United States

Unimax

DI: 04714127866239 · Model: FEC533050 · UNIMAX MEDICAL SYSTEMS INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Unimax
Primary DI
04714127866239
Version / Model
FEC533050
Company Name
UNIMAX MEDICAL SYSTEMS INC.
Labeler DUNS
658122465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-03
Public Version
1
Public Version Date
2021-03-11
Public Version Status
New
Public Device Record Key
bfa1da32-6329-464a-9ecb-6258c2db9e69

Device Description

Monopolar Forceps

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Package 14714127866236
Primary 04714127866239
Package 24714127866233