FDA UDI Not in Commercial Distribution 🇺🇸 United States

AquaLiner

DI: H787600002010 · Model: 60000201 · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AquaLiner
Primary DI
H787600002010
Version / Model
60000201
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
079105071
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2021-09-28
Public Version Status
Update
Public Device Record Key
d9d11a1d-25b9-45e8-9e68-918d3a02ba3a
Distribution End Date
2021-09-23

Device Description

AquaLiner Hydrophilic Ni-Ti Alloy Guidewire, 3cm Straight Regular Tip

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
35094 Cardiac/peripheral vascular guidewire, single-use

Identifiers

Type ID
Package H787600002015
Primary H787600002010

Customer Contacts

Device Sizes

Type Value Unit Text
Length 150 Centimeter
Outer Diameter 0.035 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
High: 27 Degrees Celsius