Vented Luer Tip Cap

GUDID 10709078008631

Vented Luer Tip Cap

WESTMED, INC.

Arterial blood sampling kit

• Primary Device ID: 10709078008631
• NIH Device Record Key: b4a250c7-bbca-4f5c-9cf2-e4c851182eaf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vented Luer Tip Cap
• Version Model Number: 0405
• Company DUNS: 092673953
• Company Name: WESTMED, INC.
• Device Count: 500
• 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: false
• 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	00709078008627 [Primary]
GS1	10709078008631 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K945454

FDA Product Code

• JKA: Tubes, Vials, Systems, Serum Separators, Blood Collection

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-25
• Device Publish Date: 2020-05-15

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