Myotech Six Series Dry Needles

GUDID 09351885000229

Myotech Dry Needles 6 Series 0.30x60mm

RED CORAL ACUPUNCTURE SUPPLIES PTY LTD

Acupuncture needle, single-use

• Primary Device ID: 09351885000229
• NIH Device Record Key: a8f2c2dd-8efc-49f6-84b2-1224035f76e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Myotech Six Series Dry Needles
• Version Model Number: RCMsix3060
• Company DUNS: 756950478
• Company Name: RED CORAL ACUPUNCTURE SUPPLIES PTY 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: true
• 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

Customer Support Contacts

• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au
• Phone: 1300240656
• Email: customerservice@redcoral.com.au

Device Identifiers

Device Issuing Agency	Device ID
GS1	09351885000229 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052731

FDA Product Code

• MQX: Needle, Acupuncture, Single Use

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2024-01-22
• Device Publish Date: 2017-06-08

On-Brand Devices [Myotech Six Series Dry Needles]

• 09351885000236: Myotech Dry Needles 6 Series 0.30x75mm
• 09351885000229: Myotech Dry Needles 6 Series 0.30x60mm
• 09351885000212: Myotech Dry Needles 6 Series 0.30x50mm
• 09351885000205: Myotech Dry Needles 6 Series 0.30x40mm