FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10653405004639 · Model: 7-796-18BX · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
NA
Primary DI
10653405004639
Version / Model
7-796-18BX
Catalog Number
7-796-18BX
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
574e9487-14e3-4dee-bc24-e98c3d210add
Distribution End Date
2023-12-05

Device Description

HANDPIECE SHEATH

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
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
12535 Medical equipment drape, single-use

Identifiers

Type ID
Primary 10653405004639
Unit of Use 00653405004632

Customer Contacts