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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

H184 — Class I MDD by Terezia Company s.r.o.

MD Atlas
Terezia Company s.r.o.

EUDAMED last updated this device on Mar 2, 2026

H184

B-SKMF000041405H184JE

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Terezia Company s.r.o.
UDI-DI code: D-SKMF000041405H184JE
Reference / catalog number: H184

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View device family (Basic UDI)

Manufacturer information

Organization name: Terezia Company s.r.o.
SRN: SK-MF-000041405
Manufacturer status: Active

Related devices

H127B-SKMF000041405H127J2On the market H201B-SKMF000041405H201HMOn the market

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW018
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW999
Nepoužívejte, pokud trpíte alergií či přecitlivělostí na některou složku tohoto výrobku.
CW999
Nepřekračujte doporučené dávkování.

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Market distribution

Primary placement in Slovakia; available across 1 country total.

Country	On market since	Until
SlovakiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-SKMF000041405H184JE
Basic UDI-DI: B-SKMF000041405H184JE
Reference / catalog number: H184
Issuing entity: EUDAMED

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC 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: 150 MU48

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

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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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.