Multichem IA Plus IA310X

GUDID 05391523440431

TECHNO-PATH MANUFACTURING LIMITED

Multiple-type clinical chemistry analyte profile IVD, control

• Primary Device ID: 05391523440431
• NIH Device Record Key: 3c457021-bf4f-4285-9618-9c80f7c09493
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multichem IA Plus
• Version Model Number: IA310X
• Catalog Number: IA310X
• 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	05391523440431 [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 Plus ]

• 05391523442190: IA320X
• 05391523442183: IA319X
• 05391523442046: 09339850190
• 05391523442039: 09339841190
• 05391523442022: 09339825190
• 05391523441988: IA318X
• 05391523441971: IA317X
• 05391523441964: IA316X
• 05391523441957: IA315MX
• 05391523441940: IA315X
• 05391523441612: IA310MX
• 05391523440745: 08P86-10
• 05391523440516: IA313A
• 05391523440509: IA312A
• 05391523440493: IA311A
• 05391523440486: IA310A
• 05391523440479: IA313X
• 05391523440462: IA312X
• 05391523440455: IA311X
• 05391523440448: IA314X
• 05391523440431: IA310X
• 05391523440004: 05P76-10