FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10653405004660 · Model: 7-796-19BX · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10653405004660
Version / Model
7-796-19BX
Catalog Number
7-796-19BX
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
6
Public Version Date
2023-06-06
Public Version Status
Update
Public Device Record Key
932dbfc2-819d-4397-aeaf-78d3b8f01c7b

Device Description

HANDPIECE SHEATH ELECTROSURGICAL

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
12535 Medical equipment drape, single-use

Identifiers

Type ID
Package 20653405004667
Primary 10653405004660

Customer Contacts