FDA UDI In Commercial Distribution 🇺🇸 United States

LumaFlex Plus Double J stent, 2 open tips, Ch/Fr7/L.28cm, without wire

DI: 03700512967699 · Model: 09-0184 · Promepla
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LumaFlex Plus Double J stent, 2 open tips, Ch/Fr7/L.28cm, without wire
Primary DI
03700512967699
Version / Model
09-0184
Catalog Number
ROJF5728ST228
Company Name
Promepla
Labeler DUNS
401020409
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-20
Public Version
2
Public Version Date
2024-01-15
Public Version Status
Update
Public Device Record Key
3d833a34-8d13-442f-868f-e934aa977009

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
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
Package 03700512987697
Package 03700512977698
Primary 03700512967699

Customer Contacts

Phone
+37797984232

Premarket Submissions

Submission Number Supplement Number
K173734 000