FDA UDI In Commercial Distribution 🇺🇸 United States

ELIMINATOR

DI: 20653405052514 · Model: 000379 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
ELIMINATOR
Primary DI
20653405052514
Version / Model
000379
Catalog Number
000379
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8dc1930f-e7ff-4bdb-89d4-60e118adb628

Device Description

CONMED ELIMINATOR 3-Stage Esophageal PET Balloon Dilator, 20mm/60F, Multipack

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KNQ Dilator, esophageal

GMDN Terms

Code Name
45712 Gastrointestinal/biliary dilation balloon catheter

Identifiers

Type ID
Package 10653405052517
Primary 20653405052514
Unit of Use 00653405052510

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033936 000

Device Sizes

Type Value Unit Text
Length 8 Millimeter
Outer Diameter 20 Centimeter
Catheter Gauge 60 French
Pressure 3400 millibar
Device Size Text, specify 2.8 Millimeter
Pressure 50 Pound per Square Inch