Huanqiu

GUDID 06956418901061

Suzhou Huanqiu Acupuncture Medical Appliance Co., Ltd.

Acupuncture needle, single-use

• Primary Device ID: 06956418901061
• NIH Device Record Key: 754ff30a-e4c9-4ce1-92fa-81ae765e0e53
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Huanqiu
• Version Model Number: 0.12×7mm
• Company DUNS: 527023772
• Company Name: Suzhou Huanqiu Acupuncture Medical Appliance 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: false
• Device Combination Product: false
• Single Use: true
• 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	06956418901061 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011242

FDA Product Code

• MQX: Needle, Acupuncture, Single Use

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-02-15

On-Brand Devices [Huanqiu]

• 06956418901061: 0.12×7mm
• 06956418900286: 0.30×25