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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

16720142003 — Class I MDR by ESPECIALIDADES MÉDICO…

MD Atlas
ESPECIALIDADES MÉDICO ORTOPEDICAS,S.L.

EUDAMED last updated this device on Nov 13, 2025

16720142003

84326791672018B

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ESPECIALIDADES MÉDICO ORTOPEDICAS,S.L.
UDI-DI code: 08432679301317
Reference / catalog number: 16720142003

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Manufacturer information

Organization name: ESPECIALIDADES MÉDICO ORTOPEDICAS,S.L.
SRN: ES-MF-000000889
Manufacturer status: Active

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: 08432679301317
Basic UDI-DI: 84326791672018B
Reference / catalog number: 16720142003
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060603FINGERS ORTHOSES

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

1672014100284326791672018BOn the market 1672014100184326791672018BOn the market 1672014200184326791672018BOn the market 1672014200284326791672018BOn the market 1672014100384326791672018BOn 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.