FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 04714127860732 · Model: 1222 · UNIMAX MEDICAL SYSTEMS INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
CONMED
Primary DI
04714127860732
Version / Model
1222
Company Name
UNIMAX MEDICAL SYSTEMS INC.
Labeler DUNS
658122465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-17
Public Version
2
Public Version Date
2020-02-17
Public Version Status
Update
Public Device Record Key
50e71165-0392-4462-b2e9-752f0ed5a7e3

Device Description

Monopolar Scissors

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
Previous 00412786063184
Package 24714127860736
Package 14714127860739
Primary 04714127860732