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SUPPORT

 

We Care about
Your Needs

Let our service convince you.

Customer Service

The SEBERS Medical customer service is perfectly tailored to the needs and wishes of our customers. Here you will receive direct, personal and competent advice when ordering a device and for all questions relating to our TMS equipment and services:
CONTACT US

Our Services

INFORMATION
You are interested in TMS or already using TMS and need more information about it? Contact us!

 

SELECTION
You have questions or need help finding the right TMS device for you? Then you have come to the right place.
FINANCING
Depending on where you are from, we have different partners that may offer you financial solutions.
PURCHASE
Purchase your machine over the phone or by email. We will inform you immediately about the expected delivery time.
PREPARATION
We keep you informed throughout the production process and prepare the delivery in advance.
DELIVERY
As standard, our systems are ready for shipment after approx. 4 weeks. We deliver them on the scheduled date.
Installation
A skilled delivery team will install the system according to the manufacturer´s specifications.
TRAINING
Our certified trainers conduct training based on your specific needs. Ask us about the next courses in your region.
SUPPORT
As our customer, you have exclusive access to our hotline for quick and uncomplicated help with questions.
MAINTENANCE
We perform regular inspections and safety checks to maintain the value and proper function of your equipment.
GERMANY
SEBERS Medical GmbH
Seidlstrasse 30
80335 Munich
Germany
+49 89 4134 0754
kontakt@sebersmedical.com
USA
SEBERS Medical Inc.
230 S Broad Street, 17th Fl
Philadelphia, PA 19102
USA
+1-833-3289-867
contact@sebersmedical.com
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© 2026 SEBERS Medical. All rights reserved.

Technology from Science – Engineered for the Patient

Disclaimer: Regulations in the United States *United States Federal Law regulates the sale of Medical Devices. The Blossom TMS Therapy System is indicated for the treatment of Major Depressive Disorder in adult patients, who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. (K220625) All other devices on this website are not approved and/or cleared for use in treatment and/or diagnosis in the United States. All investigational devices must be labeled in accordance with the labeling requirements of the IDE regulation (§ 812.5) and bear a label that states: “CAUTION. Investigational Device. Restricted by federal (or United States) law to research use.”

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