FDA UDI In Commercial Distribution 🇺🇸 United States

DURAGLIDE

DI: 20653405053757 · Model: 007145 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DURAGLIDE
Primary DI
20653405053757
Version / Model
007145
Catalog Number
007145
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
2
Public Version Date
2020-11-19
Public Version Status
Update
Public Device Record Key
013b5f15-c5b3-4a5c-b2e5-51c299a1578d

Device Description

STONE BLN 3L,15MM BELOW

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
46715 ERCP catheter, balloon, non-electrical, stone-retrieval

Identifiers

Type ID
Primary 20653405053757
Previous 00653405053753

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K993892 000

Device Sizes

Type Value Unit Text
Outer Diameter 15 Millimeter