FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 20653405010996 · Model: 60-5480-002 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
20653405010996
Version / Model
60-5480-002
Catalog Number
60-5480-002
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
89cc4825-f64e-4dd7-8acf-8448cffd49e6
Distribution End Date
2022-06-09

Device Description

EQUIPMENT CART (ASSEMBLED) ELECTROSURGICAL UNIT CART

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
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
35124 Medical device integration rack

Identifiers

Type ID
Direct Marking 10653405010999
Primary 20653405010996

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K953007 000