FDA UDI In Commercial Distribution 🇺🇸 United States

Steripath Flow

DI: 00858366007764 · Model: 5000-23UT-EN · Magnolia Medical Technologies, Inc.
Product Codes
2
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Steripath Flow
Primary DI
00858366007764
Version / Model
5000-23UT-EN
Catalog Number
5000-23UT-EN
Company Name
Magnolia Medical Technologies, Inc.
Labeler DUNS
078603710
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-25
Public Version
2
Public Version Date
2025-12-15
Public Version Status
Update
Public Device Record Key
f1995995-8399-4e34-b23b-2080be337cc2

Device Description

Steripath Flow, 23G UltraTouch, Wide Neck TA

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
FPA Set, Administration, Intravascular
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

GMDN Terms

Code Name
44903 Blood transfer set
58497 Blood collection set, invasive

Identifiers

Type ID
Package 10858366007761
Primary 00858366007764
Package 00858366007771

Premarket Submissions

Submission Number Supplement Number
K251812 000