FDA UDI In Commercial Distribution 🇺🇸 United States

NUTRIFIT

DI: 08015262020132 · Model: 1015.107 · PENTAFERTE ITALIA SRL
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NUTRIFIT
Primary DI
08015262020132
Version / Model
1015.107
Company Name
PENTAFERTE ITALIA SRL
Labeler DUNS
434304126
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-12
Public Version
1
Public Version Date
2025-03-20
Public Version Status
New
Public Device Record Key
9d3a5561-4478-487c-9f5d-fd0e362954d0

Device Description

Enteral ENFit syringe 10ml

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PNR Enteral Syringes With Enteral Specific Connectors

GMDN Terms

Code Name
59040 ENFit oral/enteral syringe, single-use

Identifiers

Type ID
Package 18015262020139
Primary 08015262020132
Package 28015262020136

Premarket Submissions

Submission Number Supplement Number
K161141 000