FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 30845854012110 · Model: E9000G · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
30845854012110
Version / Model
E9000G
Catalog Number
E9000G
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
3
Public Version Date
2021-12-13
Public Version Status
Update
Public Device Record Key
088c7c34-bb2d-4387-ba66-f71b2c7ddac7
Distribution End Date
2021-12-10

Device Description

E9000G CONTROLLER 230 VAC

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
41264 Surgical power tool system control unit, line-powered

Identifiers

Type ID
Direct Marking 20845854012113
Primary 30845854012110

Customer Contacts