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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

3060.317 — Class I MDR by OBA AG

MD Atlas
OBA AG

EUDAMED last updated this device on Apr 14, 2026

3060.317

76303184POSYZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: OBA AG
UDI-DI code: 07630318406121
Reference / catalog number: 3060.317

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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

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: 07630318406121
Basic UDI-DI: 76303184POSYZ
Reference / catalog number: 3060.317
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: Sitzbreite: 40 cm, Armauflagenhöhe: 14 cm, Inhalt: Schaumstoff, EvoPore HRC, 50 kg/m3, Bezug: oben Obatex DA aqua, RV, HG: 4, unten Obatex BR, Antirutsch, Nähte verschweisst, Länge 80 cm
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

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.