FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pro-Flo™

DI: 00613994942203 · Model: 004951 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pro-Flo™
Primary DI
00613994942203
Version / Model
004951
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-25
Public Version
4
Public Version Date
2022-09-22
Public Version Status
Update
Public Device Record Key
393d5d6e-0edf-4504-aeb5-9a6b60f9c1d8
Distribution End Date
2019-10-21

Device Description

CATH 004951 PF 10PK 6F M A RIGHT SFT TIP

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 20613994942207
Primary 00613994942203

Customer Contacts

Device Sizes

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

Storage Conditions

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