FDA UDI In Commercial Distribution 🇺🇸 United States

allSoft

DI: 00812261010069 · Model: allSoft Ureteral Stent Open Tip · ALLWIN MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
allSoft
Primary DI
00812261010069
Version / Model
allSoft Ureteral Stent Open Tip
Catalog Number
SOT5/24
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
2b7ee1e8-7867-4b91-b6fe-f2e09a6f3bc3

Device Description

allSoft Ureteral Stent Open Tip 5F, 24cm

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 10812261010066
Primary 00812261010069

Customer Contacts

Phone
714-572-1709

Premarket Submissions

Submission Number Supplement Number
K190659 000