Enteral distal end ENFit Transition Connector

GUDID 08056093721096

CEDIC SRL

ENFit/non-ISO80369-standardized linear connector

• Primary Device ID: 08056093721096
• NIH Device Record Key: 6e9bbac2-743e-4119-9155-d08c603f8e68
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Enteral distal end ENFit Transition Connector
• Version Model Number: G44989
• Company DUNS: 429471691
• Company Name: CEDIC 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056093721096 [Primary]
GS1	08056093721102 [Package]; Package: [30 Units]; In Commercial Distribution
GS1	08056093721119 [Package]; Contains: 08056093721102; Package: [24 Units]; In Commercial Distribution

FDA Product Code

• PIO: Enteral Specific Transition Connectors

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-09
• Device Publish Date: 2020-03-11

On-Brand Devices [Enteral distal end ENFit Transition Connector]

• 08056093720716: 7149 00
• 08056093720549: G44989
• 08056093721096: G44989
• 08056093720464: F00090