FDA UDI In Commercial Distribution 🇺🇸 United States

CONMED

DI: 00845854024884 · Model: 8191-11 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CONMED
Primary DI
00845854024884
Version / Model
8191-11
Catalog Number
8191-11
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2c16c005-d89f-4d02-b472-6afd535d0de1

Device Description

3DHD DUAL CHANNEL STEREO ENDOSCOPE AUTOCLAVABLE 10MM 0 DEGREE

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", "Moist Heat or Steam Sterilization"]

Product Codes

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

GMDN Terms

Code Name
12991 Ear lobe perforator

Identifiers

Type ID
Direct Marking 20845854024888
Primary 00845854024884

Customer Contacts