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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

1114-59 — Class IIa MDR by DM CEOSA

MD Atlas
DM CEOSA

EUDAMED last updated this device on Feb 25, 2026

1114-59

84356459211BJC

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DM CEOSA
UDI-DI code: 18435645900337
Reference / catalog number: 1114-59

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Manufacturer information

Organization name: DM CEOSA
SRN: ES-MF-000000579
Manufacturer status: Active

Related devices

2221-0184356459241BJTOn the market 2211-0184356459241AJROn the market 2211-0284356459241AJROn the market 2211-0384356459241AJROn the market 1131-AGL2284356459211GJNOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 18435645900337
Basic UDI-DI: 84356459211BJC
Reference / catalog number: 1114-59
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: 10
Additional product description: —
Additional information URL: https://dmceosa.com/productos-de-ortodoncia-de-calidad/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010405ORTHODONTIC WIRES

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.