Multichem IA IA302A

GUDID 05391523442299

TECHNO-PATH MANUFACTURING LIMITED

Multiple-type clinical chemistry analyte profile IVD, control

• Primary Device ID: 05391523442299
• NIH Device Record Key: ecb694e9-46ee-47ef-8176-6c88f12c6ca4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multichem IA
• Version Model Number: IA302A
• Catalog Number: IA302A
• Company DUNS: 896365983
• Company Name: TECHNO-PATH MANUFACTURING LIMITED
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05391523442299 [Primary]

FDA Product Code

• OHQ: Multi-Analyte Controls Unassayed

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: 2022-09-27
• Device Publish Date: 2022-09-19

On-Brand Devices [Multichem IA]

• 05391523442305: IA303A
• 05391523442299: IA302A
• 05391523442282: IA301A
• 05391523440738: IA300A
• 05391523440721: IA303X
• 05391523440714: IA302X
• 05391523440707: IA301X
• 05391523440691: IA300X