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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

S982 — Class I MDD by S.C. EMINVEST…

MD Atlas
S.C. EMINVEST PHARMACEUTICALS S.R.L.

EUDAMED last updated this device on Sep 16, 2024

S982

B-MINIKLIZMACHILDREN93

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: S.C. EMINVEST PHARMACEUTICALS S.R.L.
UDI-DI code: D-MINIKLIZMACHILDREN93
Reference / catalog number: S982

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View device family (Basic UDI)

Manufacturer information

Organization name: S.C. EMINVEST PHARMACEUTICALS S.R.L.
SRN: RO-MF-000001412
Manufacturer status: Active

Critical warnings

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

CW999
A lejarati ido a honap utolso napjara vonatkozik.
CW007
Ne hasznalja, ha a csomagolas serult!
CW135
Gyermekektol elzarva tartando!
CW032
A dobozon feltuntett lejarati ido utan ne alkalmazza a keszitmenyt!

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Market distribution

Primary placement in Hungary; available across 1 country total.

Placed on the market in Hungary; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: D-MINIKLIZMACHILDREN93
Basic UDI-DI: B-MINIKLIZMACHILDREN93
Reference / catalog number: S982
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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

D-MINIKLIZMACHILDREN93

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

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.