LEKON

GUDID 00807689000952

Acupuncture needles

C A I INDUSTRIES CORP

Acupuncture needle, single-use

• Primary Device ID: 00807689000952
• NIH Device Record Key: a946d18e-550d-4b8d-bca3-1d1384593442
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LEKON
• Version Model Number: NA-LK10-3060
• Company DUNS: 859060303
• Company Name: C A I INDUSTRIES CORP
• Device Count: 1000
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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	00807689000952 [Unit of Use]
GS1	00807689022503 [Primary]

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: 2020-12-07
• Device Publish Date: 2020-11-29

On-Brand Devices [LEKON]

• 00807689000914: Acupuncture needles
• 00807689000945: Acupuncture needles
• 00807689000938: Acupuncture Needles
• 00807689000921: Acupuncture needles
• 08076890200945: Acupuncture needles
• 00807689000952: Acupuncture needles