ARCHITECT 02P3610

GUDID 00380740003883

ARCHITECT HIV Ag/Ab Combo Controls

Abbott GmbH & Co. KG

HIV1/HIV2 antigen/antibody IVD, control

• Primary Device ID: 00380740003883
• NIH Device Record Key: 3da493dc-0c4c-4f1e-96ad-b33ccdc71153
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARCHITECT
• Version Model Number: 2P36-10
• Catalog Number: 02P3610
• Company DUNS: 315786293
• Company Name: Abbott GmbH & Co. KG
• 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: true
• Device Combination Product: false
• Single Use: false
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(877)422-2688
• Email: xxx@xxx.xxx
• Phone: +1(877)422-2688
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380740003883 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• BP090080

FDA Product Code

• MZF: Test, hiv detection

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-01-31

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