NUTRIFIT

GUDID 18015262039308

Enteral ENFit syringe 1ml

PENTAFERTE ITALIA SRL

ENFit oral/enteral syringe, single-use

• Primary Device ID: 18015262039308
• NIH Device Record Key: 14b50ebc-12be-4eea-8d4e-03dec0753529
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NUTRIFIT
• Version Model Number: 1015.018
• Company DUNS: 434304126
• Company Name: PENTAFERTE ITALIA SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08015262039301 [Primary]
GS1	18015262039308 [Package]; Contains: 08015262039301; Package: [100 Units]; In Commercial Distribution
GS1	28015262039305 [Package]; Package: [24 Units]; In Commercial Distribution

FDA Product Code

• PNR: Enteral Syringes With Enteral Specific Connectors

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-20
• Device Publish Date: 2025-03-12

On-Brand Devices [NUTRIFIT]

• 18015262039308: Enteral ENFit syringe 1ml
• 28015262035482: Enteral ENFit syringe 100ml
• 18015262035416: Enteral ENFit syringe 60ml
• 18015262020139: Enteral ENFit syringe 10ml
• 18015262020115: Enteral ENFit syringe 20ml
• 08015262035662: EXTENSION TUBE 150cm, for enteral use