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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

AO2018/3 — Class I MDR by Intensiv SA

MD Atlas
Intensiv SA

EUDAMED last updated this device on Feb 24, 2025

AO2018/3

++D959MANINSAODH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Intensiv SA
UDI-DI code: +D959003AO20181/
Reference / catalog number: AO2018/3

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Manufacturer information

Organization name: Intensiv SA
SRN: CH-MF-000036274
Manufacturer status: Active

Related devices

AO2018OS/3++D959MANINSAODHOn the market AO2018DS/3++D959MANINSAODHOn the market IPR-DC Set++D959MANINSIPRDCW3On the market IPR-DC050/3++D959MANINSIPRDCW3On the market IPR-DC025/3++D959MANINSIPRDCW3On 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 Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: +D959003AO20181/
Basic UDI-DI: ++D959MANINSAODH
Reference / catalog number: AO2018/3
Issuing entity: HIBCC

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 3
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010499ORTHODONTIC DEVICES - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification