FDA UDI In Commercial Distribution 🇺🇸 United States

Willow 14 Guidewire

DI: 00850076777272 · Model: USTA14ST215L09 · Arbor Endovascular LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Willow 14 Guidewire
Primary DI
00850076777272
Version / Model
USTA14ST215L09
Company Name
Arbor Endovascular LLC
Labeler DUNS
134667282
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-05
Public Version
1
Public Version Date
2025-12-15
Public Version Status
New
Public Device Record Key
a9de69f0-959b-46d6-8ab6-983ce073ee0a

Device Description

0.014 Microguidewire, Standard, Pre-shaped, 215cm, 10cm

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MOF Guide, Wire, Catheter, Neurovasculature
DQX Wire, Guide, Catheter

GMDN Terms

Code Name
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Primary 00850076777272