Sample Diluent

GUDID 06925912716617

Sample Diluent B, 45 mL×2 bottles

Shenzhen YHLO Biotech Co., Ltd.

Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD, automated/semi-automated system Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD Buffered sample diluent IVD

• Primary Device ID: 06925912716617
• NIH Device Record Key: 04eec195-7055-481b-831e-e37b82b72e2b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sample Diluent
• Version Model Number: C89912
• 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	06925912716600 [Primary]
GS1	06925912716617 [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