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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

3042.000.030 — Class I MDR by OBA AG

MD Atlas
OBA AG

EUDAMED last updated this device on Feb 19, 2025

3042.000.030

76303184POSYZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OBA AG
UDI-DI code: 07630318405483
Reference / catalog number: 3042.000.030

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Manufacturer information

Organization name: OBA AG
SRN: CH-MF-000037383
Manufacturer status: Active

Related devices

CON32.0176303184POSYZOn the market MOC93.0076303184POSYZOn the market POS74.0176303184POSYZOn the market POL10.3276303184POSYZOn the market 3001.000.00476303184ADMV9On 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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 3 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Germany		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07630318405483
Basic UDI-DI: 76303184POSYZ
Reference / catalog number: 3042.000.030
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: "R4018 Lagerungsplatte 50x50/3 cm, EvoPore HRC soft+, Bezug: Obatex Bravo, TV"
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080302PATIENT POSITIONING MEDICAL CUSHIONS

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