KingFisher™ Apex Dx 96 Combi Head

GUDID 10190302019255

LIFE TECHNOLOGIES HOLDINGS PTE. LTD.

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• Primary Device ID: 10190302019255
• NIH Device Record Key: a1799098-0f99-446f-813a-1e5d1ff08f3c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KingFisher™ Apex Dx 96 Combi Head
• Version Model Number: B24079920
• Company DUNS: 628548377
• Company Name: LIFE TECHNOLOGIES HOLDINGS PTE. LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302019255 [Primary]

FDA Product Code

• JJH: Clinical sample concentrator

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: 2023-08-11
• Device Publish Date: 2023-08-03

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