FDA UDI Not in Commercial Distribution 🇺🇸 United States

ConvertX™ Nephroureteral Stent System

DI: 00851571007499 · Model: 10.3F x 12cm · BRIGHTWATER MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ConvertX™ Nephroureteral Stent System
Primary DI
00851571007499
Version / Model
10.3F x 12cm
Catalog Number
120010-12
Company Name
BRIGHTWATER MEDICAL, INC.
Labeler DUNS
080049659
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-08
Public Version
3
Public Version Date
2021-06-08
Public Version Status
Update
Public Device Record Key
85cd0829-e3a3-41dd-80e1-8474094f5024
Distribution End Date
2021-06-07

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 00851571007499

Customer Contacts

Phone
9512903410

Device Sizes

Type Value Unit Text
Length 12 Centimeter
Catheter Gauge 10.3 French