Multichem U

GUDID 05391523440400

TECHNO-PATH MANUFACTURING LIMITED

Multiple-type clinical chemistry analyte profile IVD, control

• Primary Device ID: 05391523440400
• NIH Device Record Key: 0ff138bb-fff8-484a-a471-1446e47377ee
• Commercial Distribution Discontinuation: 2022-10-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Multichem U
• Version Model Number: UC20BX
• 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	05391523440400 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-10-20
• Device Publish Date: 2022-09-16

Devices Manufactured by TECHNO-PATH MANUFACTURING LIMITED

• 05391523442145 - Multichem IA Pus: 2024-11-13
• 05391523442152 - Multichem IA Pus: 2024-11-13
• 05391523442169 - Multichem IA Pus: 2024-11-13
• 05391523442497 - Multichem SP: 2024-03-20
• 05391523442503 - Multichem SP: 2024-03-20
• 05391523440400 - Multichem U: 2022-10-20
• 05391523440400 - Multichem U: 2022-10-20
• 05391523440868 - Multichem A1c: 2022-10-20
• 05391523440875 - Multichem A1c: 2022-10-20