Segment Sampler (SEG) A200200

GUDID 19555240401349

SEG is intended to aid extraction of a biological fluid sample from a segmented piece of tubing.

ITL ASIA PACIFIC SDN. BHD.

Blood donor bag segment sampling IVD

• Primary Device ID: 19555240401349
• NIH Device Record Key: 2a6159a5-7a4a-4ea8-ab8f-0fd01b1b9665
• Commercial Distribution Discontinuation: 2024-03-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Segment Sampler (SEG)
• Version Model Number: A200200
• Catalog Number: A200200
• Company DUNS: 597723837
• Company Name: ITL ASIA PACIFIC SDN. BHD.
• 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: true
• 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

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

Operating and Storage Conditions

• 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	19555240401332 [Primary]
GS1	19555240401349 [Package]; Contains: 19555240401332; Package: Inner Box [60 Units]; Discontinued: 2024-03-11; Not in Commercial Distribution
GS1	19555240401356 [Package]; Package: Carton [6 Units]; Discontinued: 2024-03-11; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• BK170102

FDA Product Code

• KSS: Supplies, Blood-Bank

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-08-08
• Device Publish Date: 2020-09-19

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