SampLok® Adapter Cap Insert A100709

GUDID 19555240400021

SampLok® Adaptor Cap Insert (an optional accessory) can be locked into place inside SampLok® Adaptor Cap to facilitate collection of blood sample into vacuum tube(s). It is a single use device.

ITL ASIA PACIFIC SDN. BHD.

Blood collection tube holder, single-use

• Primary Device ID: 19555240400021
• NIH Device Record Key: 4f83f03c-2feb-4775-b2ea-a2875573c42d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SampLok® Adapter Cap Insert
• Version Model Number: A100709
• Catalog Number: A100709
• Company DUNS: 597723837
• Company Name: ITL ASIA PACIFIC SDN. BHD.
• Device Count: 50
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com
• Phone: +18884112851
• Email: sales@itlbiomedical.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Away From Direct Sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	09555240400017 [Unit of Use]
GS1	19555240400014 [Primary]
GS1	19555240400021 [Package]; Contains: 19555240400014; Package: Carton [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000777

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-04-23
• Device Publish Date: 2019-03-29

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