Ultimate rTMS

GUDID 06971538580033

Stimulator

Shenzhen Yingzhi Technology Co.,Ltd.

Magnetic neural stimulation system

• Primary Device ID: 06971538580033
• NIH Device Record Key: bed1db81-6d3b-463f-a60e-3092517a2719
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultimate rTMS
• Version Model Number: M-30 Ultimate
• Company DUNS: 560014166
• Company Name: Shenzhen Yingzhi Technology Co.,Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com
• Phone: 400-999-8239
• Email: support@yingchitech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971538580033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230735

FDA Product Code

• OBP: Transcranial Magnetic Stimulator

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: 2024-01-24
• Device Publish Date: 2024-01-16

On-Brand Devices [Ultimate rTMS]

• 06971538580040: M-10 Ultimate
• 06971538580026: Stimulator
• 06971538580033: Stimulator
• 06971538580019: Stimulator