Multichem IA Pus IA323A

GUDID 05391523442169

TECHNO-PATH MANUFACTURING LIMITED

Multiple-type clinical chemistry analyte profile IVD, control

• Primary Device ID: 05391523442169
• NIH Device Record Key: b027bc7f-ee41-454a-a2dd-f4eb78c23d2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multichem IA Pus
• Version Model Number: IA323A
• Catalog Number: IA323A
• 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: true
• 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	05391523442169 [Primary]

FDA Product Code

• JJY: Multi-Analyte Controls, All Kinds (Assayed)

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: 2024-11-13
• Device Publish Date: 2024-11-05

On-Brand Devices [Multichem IA Pus ]

• 05391523442169: IA323A
• 05391523442152: IA322A
• 05391523442145: IA321A