FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00858778006379 · Model: P1UVC-2530 · FOOTPRINT MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00858778006379
Version / Model
P1UVC-2530
Company Name
FOOTPRINT MEDICAL, INC.
Labeler DUNS
791238046
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-20
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
0200fa50-ae2c-49b5-a223-947c8df6cc67

Device Description

2.5Fr Single Lumen Polyurethane Umbilical Catheter

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FOS Catheter, Umbilical Artery

GMDN Terms

Code Name
10759 Umbilical catheter

Identifiers

Type ID
Package 10858778006376
Primary 00858778006379

Customer Contacts

Phone
2102262600

Premarket Submissions

Submission Number Supplement Number
K120304 000

Device Sizes

Type Value Unit Text
Catheter Gauge 2.5 French