Enteral Distal End ENFit Transition Connector

GUDID 08056093720464

CEDIC SRL

ENFit/non-ISO80369-standardized linear connector

• Primary Device ID: 08056093720464
• NIH Device Record Key: a379a3d5-dd61-4464-8b03-6e686be93078
• Commercial Distribution Discontinuation: 2021-10-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Enteral Distal End ENFit Transition Connector
• Version Model Number: F00090
• 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	08056093720327 [Primary]
GS1	08056093720334 [Package]; Contains: 08056093720327; Package: [10 Units]; Discontinued: 2021-10-11; Not in Commercial Distribution
GS1	08056093720464 [Package]; Contains: 08056093720334; Package: [80 Units]; Discontinued: 2021-10-11; Not 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: 2021-10-12
• Device Publish Date: 2018-05-04

On-Brand Devices [Enteral Distal End ENFit Transition Connector]

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