FDA UDI In Commercial Distribution 🇺🇸 United States

JFil® Ureteral Suture Stent

DI: 03700512968344 · Model: ROJV5708ST · Promepla
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
JFil® Ureteral Suture Stent
Primary DI
03700512968344
Version / Model
ROJV5708ST
Catalog Number
JFCS80
Company Name
Promepla
Labeler DUNS
401020409
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-04-06
Public Version
1
Public Version Date
2022-04-14
Public Version Status
New
Public Device Record Key
ed7dac7b-461b-4693-aa18-18a142e3b94e

Device Description

Comfort Stent 7Fr - 80mm

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
Yes
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
Yes

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
Package 03700512978343
Primary 03700512968344
Package 03700512988342