Digest-All™ 4 (Proteinase K Solution)

GUDID 10190302007542

LIFE TECHNOLOGIES CORPORATION

Buffered sample diluent IVD, manual

• Primary Device ID: 10190302007542
• NIH Device Record Key: 42fa4c3e-05bb-48ef-9ed3-df3e95c15023
• Commercial Distribution Discontinuation: 2022-04-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Digest-All™ 4 (Proteinase K Solution)
• Version Model Number: 003011
• 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	10190302007542 [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: 2022-05-23
• Device Publish Date: 2018-02-02

Devices Manufactured by LIFE TECHNOLOGIES CORPORATION

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