FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 20653405004636 · Model: 7-796-18BX · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
CONMED
Primary DI
20653405004636
Version / Model
7-796-18BX
Catalog Number
7-796-18BX
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-12-05
Public Version
1
Public Version Date
2023-12-13
Public Version Status
New
Public Device Record Key
ddba5650-21fb-44e2-a364-6d922f3550b6

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
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
12535 Medical equipment drape, single-use

Identifiers

Type ID
Unit of Use 00653405004632
Primary 20653405004636
Previous 10653405004639

Customer Contacts