FDA UDI In Commercial Distribution 🇺🇸 United States

Foundation DRS Solo

DI: 00850047730336 · Model: FS1-0404 · Bionova Medical Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Foundation DRS Solo
Primary DI
00850047730336
Version / Model
FS1-0404
Company Name
Bionova Medical Inc.
Labeler DUNS
080325588
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-17
Public Version
1
Public Version Date
2025-09-25
Public Version Status
New
Public Device Record Key
b2264b55-9e06-4880-b76b-1ca98d065e55

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
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
FTM Mesh, Surgical
PMQ Peripheral Blood Processing Device For Wound Management
QSZ Absorbable Synthetic Wound Dressing
FRO Dressing, Wound, Drug

GMDN Terms

Code Name
58071 Wound regenerating polysaccharide agent

Identifiers

Type ID
Primary 00850047730336

Customer Contacts

Phone
901-7482581

Device Sizes

Type Value Unit Text
Length 4 Centimeter
Width 4 Centimeter