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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

6070.207.55.F — Class I MDR by Fabricados Triton, S.L.

MD Atlas
Fabricados Triton, S.L.

EUDAMED last updated this device on Nov 18, 2024

6070.207.55.F

8424591CMUU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fabricados Triton, S.L.
UDI-DI code: 8424591607158
Reference / catalog number: 6070.207.55.F

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Manufacturer information

Organization name: Fabricados Triton, S.L.
SRN: ES-MF-000018967
Manufacturer status: Inactive

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 8424591607158
Basic UDI-DI: 8424591CMUU
Reference / catalog number: 6070.207.55.F
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: 1
Additional product description: Camilla Blanca 180X55X70 Con Hueco Facial
Additional information URL: http://fabricadostriton.com/14-camillas
Clinical sizes: No clinical sizes registered for this device.

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

Related devices

6060.206.558424591CMUUOn the market 6060.206.55.F8424591CMUUOn the market 6070.207.558424591CMUUOn the market 6080.208.558424591CMUUOn the market 6060.206.608424591CMUUOn 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.