LUER SLIP DISC FILTER (FEMALE TO LUER SLIP)

GUDID 05055788761945

FLEXICARE MEDICAL LIMITED

Hydrophobic Luer filter, non-sterile

• Primary Device ID: 05055788761945
• NIH Device Record Key: 095d1065-dcc7-4c45-b0d5-a6a2e07d0a66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUER SLIP DISC FILTER (FEMALE TO LUER SLIP)
• Version Model Number: 010-741U
• Company DUNS: 504406273
• Company Name: FLEXICARE MEDICAL LIMITED
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055788761945 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133516

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
• JRL: Unit, Filter, Membrane

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-09
• Device Publish Date: 2016-10-10

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