FDA UDI In Commercial Distribution 🇺🇸 United States

ADx Guidewire

DI: 15051684019132 · Model: H7878105382600 · Angiodynamics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
ADx Guidewire
Primary DI
15051684019132
Version / Model
H7878105382600
Catalog Number
810538260
Company Name
Angiodynamics, Inc.
Labeler DUNS
079252781
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-11
Public Version
2
Public Version Date
2025-03-06
Public Version Status
Update
Public Device Record Key
bbb6f63d-372d-4fc3-b718-32b0579e33f5

Device Description

GUIDEWIRE, PTFE 038 X 260CM FC 3MM J

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
DQX Wire, guide, catheter

GMDN Terms

Code Name
58115 Peripheral vascular guidewire, manual

Identifiers

Type ID
Primary 15051684019132
Previous H7878105382600
Package 25051684019139

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify .038" x 260cm x 3mmJ
Outer Diameter 0.038 Inch
Length 260 Centimeter