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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

2200 EP S3 TT V2 — Class I MDR by SOLTEC S.r.l.

MD Atlas
SOLTEC S.r.l.

EUDAMED last updated this device on May 26, 2026

2200 EP S3 TT V2

805108418FT002ST2M

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SOLTEC S.r.l.
UDI-DI code: 08051084181408
Reference / catalog number: 2200 EP S3 TT V2

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View device family (Basic UDI)

Manufacturer information

Organization name: SOLTEC S.r.l.
SRN: IT-MF-000018179
Manufacturer status: Active

Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030140-00Issued
Quality management systemNotified body: 0425Expiry: Jul 30, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 2 countries total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market
Hungary		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08051084181408
Basic UDI-DI: 805108418FT002ST2M
Reference / catalog number: 2200 EP S3 TT V2
Issuing entity: GS1

Classification

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

Device details

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08051084181408

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12011302ULTRASONIC CLEANING EQUIPMENT

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

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