EXEL Multi Sample Luer Adapter 26537

GUDID 30020221265379

Luer Adapter

Exel International

Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike Luer-ended blood collection tube spike

• Primary Device ID: 30020221265379
• NIH Device Record Key: f1c24865-3915-461c-84d2-cb3e22794835
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXEL Multi Sample Luer Adapter
• Version Model Number: 26537
• Catalog Number: 26537
• Company DUNS: 180572216
• Company Name: Exel International
• Device Count: 100
• 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	00020221265378 [Unit of Use]
GS1	10020221265375 [Primary]
GS1	20020221265372 [Package]; Contains: 10020221265375; Package: [10 Units]; In Commercial Distribution
GS1	30020221265379 [Package]; Contains: 20020221265372; Package: [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K861152

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-09-23

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