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

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Organization name
UDI-DI code
Reference / catalog number

A498/4 — Class IIb MDR by Termosalud, S.L.

MD Atlas
Termosalud, S.L.

EUDAMED last updated this device on Feb 4, 2026

A498/4

843660129ZPEMSHP4H6

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Termosalud, S.L.
UDI-DI code: 08436601291400
Reference / catalog number: A498/4

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Manufacturer information

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

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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: not provided
UDI-DI code: 08436601291400
Basic UDI-DI: 843660129ZPEMSHP4H6
Reference / catalog number: A498/4
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: ELECTROSTIMULATION HANDPIECE 4
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

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

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.