iFlash-Cleaning Solution

GUDID 06925912716471

45 mL×2 bottles

Shenzhen YHLO Biotech Co., Ltd.

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• Primary Device ID: 06925912716471
• NIH Device Record Key: 855215be-11e5-4737-82a0-30440603fc58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iFlash-Cleaning Solution
• Version Model Number: C80003
• 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	06925912716471 [Primary]
GS1	06925912716488 [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 [iFlash-Cleaning Solution]

• 06925912716471: 45 mL×2 bottles
• 06925912716501: 30 mL×2 bottles