FDA UDI Not in Commercial Distribution 🇺🇸 United States

PRO-FLO™

DI: 00613994939142 · Model: 07PF029 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRO-FLO™
Primary DI
00613994939142
Version / Model
07PF029
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
2019-01-15
Public Version Status
Update
Public Device Record Key
255e9c3f-5d49-4ac5-ba40-3e0018c33262
Distribution End Date
2018-10-05

Device Description

CATHETER 07PF029 PF 5PK 7F BERNSTEIN 110

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 20613994939146
Primary 00613994939142

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960056 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 1.55 Millimeter
Length 110.0 Centimeter
Catheter Gauge 7.0 French

Storage Conditions

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