FDA UDI In Commercial Distribution 🇺🇸 United States

Angiographic Guide Wire

DI: 00643169856950 · Model: 007648 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Angiographic Guide Wire
Primary DI
00643169856950
Version / Model
007648
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-19
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
6c224f9e-846c-4b0a-b5b7-d1abaa8fe0ac

Device Description

WIRE ANG 007648 10PK 9315S.032 120 3MMJT

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
No
Has Expiration Date
No
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 20643169856954
Primary 00643169856950

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082873 000

Device Sizes

Type Value Unit Text
Length 120.0 Centimeter
Outer Diameter 0.813 Millimeter