FDA UDI Not in Commercial Distribution 🇺🇸 United States

CONMED

DI: 20845854038823 · Model: 8170-9 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CONMED
Primary DI
20845854038823
Version / Model
8170-9
Catalog Number
8170-9
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
2022-06-10
Public Version Status
Update
Public Device Record Key
b03eba1a-eac5-40de-b501-a6e531e48c54
Distribution End Date
2022-06-09

Device Description

3DHD DUAL CHANNEL CAMERA HEAD

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FET Endoscopic video imaging system/component, gastroenterology-urology

GMDN Terms

Code Name
35958 Endoscope video camera

Identifiers

Type ID
Direct Marking 30845854038820
Primary 20845854038823

Customer Contacts