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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

BETTER — Class I MDR by MG TEC INDUSTRY DEJ

MD Atlas
MG TEC INDUSTRY DEJ

EUDAMED last updated this device on Nov 8, 2024

BETTER

594071420BETTERCEARSAFWH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MG TEC INDUSTRY DEJ
UDI-DI code: 05940714200004
Reference / catalog number: 160144006

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View device family (Basic UDI)

Manufacturer information

Organization name: MG TEC INDUSTRY DEJ
SRN: RO-MF-000043568
Manufacturer status: Active

Related devices

BETTER594071420BETTERSCUTEC01JVOn the market BETTER594071420BETTERSCUTEC01JVOn the market BETTER594071420BETTERSCUTEC01JVOn the market BETTER594071420BETTERSCUTEC00JTOn the market BETTER594071420BETTERSCUTEC00JTOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: BETTER
UDI-DI code: 05940714200004
Basic UDI-DI: 594071420BETTERCEARSAFWH
Reference / catalog number: 160144006
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: Underpad designed to provide discreet and effective protection for adults experiencing urinary or fecal incontinence, 60X90cm, 30 pcs.
Additional information URL: https://www.mgtecindustry.ro/
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)05940714200004

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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.

T04010201UNTUCKABLE UNDERPADS

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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