FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 20653405003271 · Model: 138019 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
5

Basic Information

Brand Name
CONMED
Primary DI
20653405003271
Version / Model
138019
Catalog Number
138019
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-12-01
Public Version
1
Public Version Date
2023-12-11
Public Version Status
New
Public Device Record Key
8c577365-a760-440f-8be3-013743a31737

Device Description

1/8" BALL ELECTRODE

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
45686 Electrosurgical handpiece/electrode holder, single-use

Identifiers

Type ID
Unit of Use 00653405003277
Direct Marking 30653405003278
Previous 10653405003274
Primary 20653405003271

Customer Contacts