Extension line doble Luer Lock 1.7x3.0x23mm ODG0015USST

GUDID 03700512925200

Promepla

Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose Fluid transfer set, general-purpose

• Primary Device ID: 03700512925200
• NIH Device Record Key: 2a68f3de-a3db-4775-bfb1-3f6ab2c7d90d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Extension line doble Luer Lock 1.7x3.0x23mm
• Version Model Number: ODG0015USST
• Catalog Number: ODG0015USST
• Company DUNS: 401020409
• Company Name: Promepla
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700512925200 [Package]; Contains: 03700512952022; Package: BOX [100 Units]; In Commercial Distribution
GS1	03700512952022 [Primary]

FDA Product Code

• KYX: Dispenser, Liquid Medication

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: 2020-04-13
• Device Publish Date: 2020-04-03

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