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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

Dom'Hous — Class I MDR by Karapharm

MD Atlas
Karapharm

EUDAMED last updated this device on Sep 12, 2022

Dom'Hous

376036425ACARHOUSSESPJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Karapharm
UDI-DI code: 37603642506080
Reference / catalog number: 201008

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Manufacturer information

Organization name: Karapharm
SRN: FR-MF-000006596
Manufacturer status: Active

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Acar Housses376036425ACARHOUSSESPJOn the market Acar Housses376036425ACARHOUSSESPJOn the market Acar Housses376036425ACARHOUSSESPJOn the market Acar Housses376036425ACARHOUSSESPJOn the market Acar Housses376036425ACARHOUSSESPJOn the market

Critical warnings

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

CW011
NE PAS LAISSER A PORTEE DES ENFANTS
CW010
NE PAS UTILISER DE CUTTER ET DE POINTES

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: Dom'Hous
UDI-DI code: 37603642506080
Basic UDI-DI: 376036425ACARHOUSSESPJ
Reference / catalog number: 201008
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: Dom'Hous Enveloppe couette 140x200 cm
Additional information URL: https://stallergenesgreer.fr/commander-des-housses-anti-acariens-dispositifs-medicaux
Clinical sizes: 200 MU10
140 MU10

EMDN nomenclature code(s)

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

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.