FDA UDI In Commercial Distribution 🇺🇸 United States

ELIMINATOR

DI: 20653405050909 · Model: 000347 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ELIMINATOR
Primary DI
20653405050909
Version / Model
000347
Catalog Number
000347
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-16
Public Version
1
Public Version Date
2020-10-26
Public Version Status
New
Public Device Record Key
b5ccb737-19c8-4e10-a42a-c0adff0aca91

Device Description

BILIARY BALLOON DILATOR 4MM2CM

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FGE Stents, drains and dilators for the biliary ducts

GMDN Terms

Code Name
45712 Gastrointestinal/biliary dilation balloon catheter

Identifiers

Type ID
Previous 00653405050905
Primary 20653405050909

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K920361 000

Device Sizes

Type Value Unit Text
Pressure 150 Pound per Square Inch