FDA UDI In Commercial Distribution 🇺🇸 United States

Amplatzer™

DI: 00811806010724 · Model: Guidewire · AGA MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Amplatzer™
Primary DI
00811806010724
Version / Model
Guidewire
Catalog Number
9-GW-002
Company Name
AGA MEDICAL CORPORATION
Labeler DUNS
966215829
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-04
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6413752a-9f99-41d4-9043-9879f8cd186c

Device Description

Guidewire

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
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
Primary 00811806010724

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.889 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry.