FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 00613994885005 · Model: 010439 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00613994885005
Version / Model
010439
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
3
Public Version Date
2019-03-11
Public Version Status
Update
Public Device Record Key
8e681764-cc0a-4018-872e-6347f40d2fdb
Distribution End Date
2018-10-05

Device Description

GUIDEWIRE ANGIO 010439 .025X45 STR FC SS

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
Yes
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 20613994885009
Primary 00613994885005

Customer Contacts

Device Sizes

Type Value Unit Text
Length 45.0 Centimeter
Outer Diameter 0.635 Millimeter