FDA UDI In Commercial Distribution 🇺🇸 United States

Pro-Flo XT™

DI: 00613994944573 · Model: 060048 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Flo XT™
Primary DI
00613994944573
Version / Model
060048
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-13
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3cefae3a-1eee-4d19-a61b-59dd4f609bec

Device Description

CATH 060048 PF 10PK 6F XT PIG SF TP 125

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
DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 20613994944577
Primary 00613994944573

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960056 000

Device Sizes

Type Value Unit Text
Catheter Gauge 6.0 French
Lumen/Inner Diameter 1.27 Millimeter
Length 125.0 Centimeter

Storage Conditions

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