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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

C103P — Class I MDR by Inter.med

MD Atlas
Inter.med

EUDAMED last updated this device on Sep 24, 2024

C103P

37601BATFW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Inter.med
UDI-DI code: 03760139501904
Reference / catalog number: C103P

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Manufacturer information

Organization name: Inter.med
SRN: FR-MF-000000461
Manufacturer status: Active

Related devices

ASPIROBAT®37601ORAJCOn the market C355S37601ORAJCOn the market C347S, C347, C345, C345S37601TUBKGOn the market BATO-NEZ37601BATFWOn the market CN0137601BATFWOn the market

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760139501904
Basic UDI-DI: 37601BATFW
Reference / catalog number: C103P
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: BÂTONNET SOINS DE BOUCHE USAGE UNIQUE MOUSSE BLANCHE GRAND CÔNE MANCHE PLASTIQUE 15CM RIGIDE SACHET DE 10 - BOITE DE 100 (10x10)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y0999PERSONAL CARE AIDS - 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.