FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20653405009198 · Model: 60-5104-001 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
20653405009198
Version / Model
60-5104-001
Catalog Number
60-5104-001
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-10
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
ca1fa93c-bd26-4e86-afa8-d38d064f0f4e

Device Description

FOOTSWITCH MONOPOLAR DOUBLE TREADLE

Device Characteristics

Single Use
No
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
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
Previous 30653405009195
Primary 20653405009198

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K810101 000