FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00859950007504 · Model: P1FTM5.0-EN · FOOTPRINT MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00859950007504
Version / Model
P1FTM5.0-EN
Company Name
FOOTPRINT MEDICAL, INC.
Labeler DUNS
791238046
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-29
Public Version
1
Public Version Date
2022-10-07
Public Version Status
New
Public Device Record Key
ad31d3aa-9b52-42a3-b87b-4d9c76ac14c2

Device Description

Polyurethane Feeding Tube with male Enteral Connector 5.0Fr by 60cm

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
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
14221 Nasogastric feeding tube

Identifiers

Type ID
Package 10859950007501
Primary 00859950007504

Customer Contacts

Phone
2102262600

Premarket Submissions

Submission Number Supplement Number
K102548 000

Device Sizes

Type Value Unit Text
Length 60 Centimeter
Catheter Gauge 5.0 French