FDA UDI In Commercial Distribution 🇺🇸 United States

NUTRIFIT

DI: 08015262035662 · Model: 368.1572 · PENTAFERTE ITALIA SRL
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NUTRIFIT
Primary DI
08015262035662
Version / Model
368.1572
Company Name
PENTAFERTE ITALIA SRL
Labeler DUNS
434304126
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-03
Public Version
1
Public Version Date
2025-07-11
Public Version Status
New
Public Device Record Key
56021f22-5607-4438-a076-96b84b8951ba

Device Description

EXTENSION TUBE 150cm, for enteral use

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FPD Tube, Feeding
KNT Tubes, Gastrointestinal (And Accessories)

GMDN Terms

Code Name
62256 Enteral tube extension, single-use

Identifiers

Type ID
Primary 08015262035662
Package 28015262035666