FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00613994964502 · Model: 001372 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00613994964502
Version / Model
001372
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-05
Public Version
3
Public Version Date
2020-03-30
Public Version Status
Update
Public Device Record Key
251fe4b0-cf43-4df1-8846-5eca2d599c91

Device Description

WVN CATH 001372 10PK 7F 125CM

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
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 20613994964506
Primary 00613994964502

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 7.0 French
Lumen/Inner Diameter 1.295 Millimeter
Length 125.0 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store catheters in a cool, dry area.