Sample Diluent

GUDID 06925912716709

Sample Diluent I, 45 mL×2 bottles

Shenzhen YHLO Biotech Co., Ltd.

Buffered sample diluent IVD, automated/semi-automated system

• Primary Device ID: 06925912716709
• NIH Device Record Key: a4bdffae-5817-44e6-9dd0-8ab376eff569
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sample Diluent
• Version Model Number: C89919
• Company DUNS: 420735989
• Company Name: Shenzhen YHLO Biotech Co., Ltd.
• Device Count: 2
• 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: true
• 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	06925912716693 [Primary]
GS1	06925912716709 [Unit of Use]

FDA Product Code

• PPM: General Purpose Reagent

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: 2022-11-03
• Device Publish Date: 2022-10-26

On-Brand Devices [Sample Diluent]

• 06925912716785: Sample Diluent I-1, 0.57 mL×100 PCS
• 06925912716709: Sample Diluent I, 45 mL×2 bottles
• 06925912716686: Sample Diluent H, 45 mL×2 bottles
• 06925912716655: Sample Diluent G, 45 mL×2 bottles
• 06925912716662: Sample Diluent D, 45 mL×2 bottles
• 06925912716778: Sample Diluent D, 120 microliter x100 PCS
• 06925912716617: Sample Diluent B, 45 mL×2 bottles
• 06925912716594: Sample Diluent A, 45 mL×2 bottles