FDA UDI In Commercial Distribution 🇺🇸 United States

Bard® InLay® Ureteral Stent

DI: 00801741014932 · Model: 778814 · C. R. Bard, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bard® InLay® Ureteral Stent
Primary DI
00801741014932
Version / Model
778814
Catalog Number
778814
Company Name
C. R. Bard, Inc.
Labeler DUNS
016898496
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7594b251-b477-4306-80ab-fd32da2b4fa7

Device Description

INLAY URETERAL STENT w/o GUIDEWIRE

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
No

Product Codes

Code Name
FAD STENT, URETERAL

GMDN Terms

Code Name
58005 Polymeric ureteral stent

Identifiers

Type ID
Primary 00801741014932

Customer Contacts

Device Sizes

Type Value Unit Text
Length 14 Centimeter
Catheter Gauge 8 French