Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

ZIONIC PRO MAX — Class IIb MDR by Termosalud, S.L.

MD Atlas
Termosalud, S.L.

EUDAMED last updated this device on Feb 4, 2026

ZIONIC PRO MAX

843660129ZPMQ7

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Termosalud, S.L.
UDI-DI code: 08436601291448
Reference / catalog number: M105/1

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Termosalud, S.L.
SRN: ES-MF-000019177
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Refer to the instructions for use for detailed information on critical warnings and contraindications before operating the device

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Dec 16, 2025	Still on market

Device identification

Trade name: ZIONIC PRO MAX
UDI-DI code: 08436601291448
Basic UDI-DI: 843660129ZPMQ7
Reference / catalog number: M105/1
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: RADIOFREQUENCY AND ELECTROSTIMULATION DEVICE
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12040203DERMAL REGENERATION EQUIPMENT
Z12062801MUSCLE REINFORCEMENT STIMULATORS FOR INNERVATED MUSCLES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

M92AE843660129CRIOTSJ9On the market M91AE843660129LASTSMDU9On the market PLATE 19D843660129CSPMDEUOn the market M85AEN843660129SYMMEDTSKLOn the market M85AE843660129SYMMEDTSKLOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.