invitrogen

GUDID 10190302000130

LIFE TECHNOLOGIES CORPORATION

Streptavidin-enzyme conjugate reagent IVD

• Primary Device ID: 10190302000130
• NIH Device Record Key: 92b0a8b4-f13c-4031-8fdb-d7460feb7354
• Commercial Distribution Discontinuation: 2018-06-15
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: invitrogen
• Version Model Number: 879263
• Company DUNS: 080131636
• Company Name: LIFE TECHNOLOGIES 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302000130 [Primary]

FDA Product Code

• NJT: IMMUNOHISTOCHEMISTRY REAGENTS AND KITS

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-10-18
• Device Publish Date: 2016-08-01

On-Brand Devices [invitrogen]

• 10190302000130: 879263
• 10190302000123: 878973