FDA UDI In Commercial Distribution 🇺🇸 United States

Pro-Flo™

DI: 00613994943033 · Model: 010023 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Flo™
Primary DI
00613994943033
Version / Model
010023
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
6ae3b261-acdc-4310-bb2b-532e1a5abd5a

Device Description

CATH 010023 PF 10PK 6F SOFT TIP ALII

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 20613994943037
Primary 00613994943033

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K960056 000

Device Sizes

Type Value Unit Text
Length 100.0 Centimeter
Catheter Gauge 6.0 French
Lumen/Inner Diameter 1.27 Millimeter

Storage Conditions

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