LUYAO

GUDID 06940979190033

Zhejiang Luyao Electronics Technology Co., Ltd.

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• Primary Device ID: 06940979190033
• NIH Device Record Key: 63298ae8-9d72-448f-ac1e-49d4797e594c
• Commercial Distribution Discontinuation: 2073-08-29
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUYAO
• Version Model Number: LY-670D
• Company DUNS: 528189371
• Company Name: Zhejiang Luyao Electronics Technology Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	06940979190033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222949

FDA Product Code

• IPR: Crutch

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: 2023-09-06
• Device Publish Date: 2023-08-29