FDA UDI In Commercial Distribution 🇺🇸 United States

Angiographic Guide Wire

DI: 00613994885203 · Model: 994802 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Angiographic Guide Wire
Primary DI
00613994885203
Version / Model
994802
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-18
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0126e5b5-5df8-4a7f-ba71-f9ea43379016

Device Description

WIRE ANGIO 994802 0.21 X180CM 3MMJ PTFE

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 20613994885207
Primary 00613994885203

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082873 000

Device Sizes

Type Value Unit Text
Length 180.0 Centimeter
Outer Diameter 0.533 Millimeter