Pre-Trigger Solution (1×)

GUDID 06925912716532

500 mL×4 bottles

Shenzhen YHLO Biotech Co., Ltd.

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• Primary Device ID: 06925912716532
• NIH Device Record Key: eed91bf4-98c3-471e-92ae-cd0a12998307
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pre-Trigger Solution (1×)
• Version Model Number: C89959
• Company DUNS: 420735989
• Company Name: Shenzhen YHLO Biotech Co., Ltd.
• Device Count: 4
• 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	06925912716112 [Primary]
GS1	06925912716532 [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 [Pre-Trigger Solution (1×)]

• 06925912716549: 220 mL×4 bottles
• 06925912716532: 500 mL×4 bottles
• 06925912716525: 900 mL×4 bottles