R. KDY Pack 4 WELL 2001

GUDID 00813545020293

SCIMEDX CORPORATION

Mitochondrial antibody M2 (anti-Mi2) IVD, kit, fluorescent immunoassay Mitochondrial antibody M2 (anti-Mi2) IVD, kit, fluorescent immunoassay

• Primary Device ID: 00813545020293
• NIH Device Record Key: b3504650-b4c2-4446-866e-d428fa2dc795
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: R. KDY Pack 4 WELL
• Version Model Number: 2001
• Catalog Number: 2001
• Company DUNS: 155424708
• Company Name: SCIMEDX CORPORATION
• 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

Customer Support Contacts

• Phone: 18002215598
• Email: service@scimedx.com
• Phone: 18002215598
• Email: service@scimedx.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813545020293 [Primary]

FDA Product Code

• DBM: Antimitochondrial Antibody, Indirect Immunofluorescent, Antigen, Control

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: 2018-03-29
• Device Publish Date: 2016-09-13

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