FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pro-Flo XT™

DI: 00613994942708 · Model: 010162 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Flo XT™
Primary DI
00613994942708
Version / Model
010162
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-13
Public Version
4
Public Version Date
2022-09-22
Public Version Status
Update
Public Device Record Key
dd238084-3b20-4c14-9ba6-30ab395d0b69
Distribution End Date
2019-10-21

Device Description

CATH 010162 PF 10PK 7F XT JL6 SF TP 100

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 20613994942702
Primary 00613994942708

Customer Contacts

Device Sizes

Type Value Unit Text
Length 100.0 Centimeter
Catheter Gauge 7.0 French
Lumen/Inner Diameter 1.55 Millimeter

Storage Conditions

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