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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

C355S — Class IIa MDR by Inter.med

MD Atlas
Inter.med

EUDAMED last updated this device on Jun 13, 2023

C355S

37601ORAJC

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Inter.med
UDI-DI code: 03760139503458
Reference / catalog number: C355S

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Manufacturer information

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

Related devices

ASPIROBAT®37601ORAJCOn the market C347S, C347, C345, C345S37601TUBKGOn the market BATO-NEZ37601BATFWOn the market CN0137601BATFWOn the market SCD7037601BATFWOn 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.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Oct 14, 2017	Oct 13, 2022

Device identification

Trade name: not provided
UDI-DI code: 03760139503458
Basic UDI-DI: 37601ORAJC
Reference / catalog number: C355S
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
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)

Q019003DENTAL FLOSS AND OTHER DEVICES FOR ORAL HYGIENE (FOR PROFESSIONAL USE)

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