FDA UDI In Commercial Distribution 🇺🇸 United States

R+

DI: 00812261011950 · Model: R+ Urinary Diversion Stents [Mono - J] Open Tip 7F, 70cm with Guidewire · ALLWIN MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
R+
Primary DI
00812261011950
Version / Model
R+ Urinary Diversion Stents [Mono - J] Open Tip 7F, 70cm with Guidewire
Catalog Number
MJO-7/70-R+-G
Company Name
ALLWIN MEDICAL DEVICES, INC.
Labeler DUNS
796354509
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-09
Public Version
1
Public Version Date
2024-01-17
Public Version Status
New
Public Device Record Key
b569eedc-2474-44cf-bc72-c2142b1edf86

Device Description

R+ Urinary Diversion Stents [Mono - J] Open Tip 7F, 70cm with Guidewire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
Package 10812261011957
Primary 00812261011950

Customer Contacts

Phone
714-512-1709

Premarket Submissions

Submission Number Supplement Number
K190659 000