FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 20653405002144 · Model: 130146 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
CONMED
Primary DI
20653405002144
Version / Model
130146
Catalog Number
130146
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-11
Public Version
1
Public Version Date
2023-10-19
Public Version Status
New
Public Device Record Key
d2a0713e-d690-45de-8d8a-045067ef520d

Device Description

ELECTROSURGICAL FOOTSWITCH

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
44774 Inert gas-enhanced electrosurgical system

Identifiers

Type ID
Direct Marking 10653405002147
Previous 30653405002141
Primary 20653405002144

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K933332 000