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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

08437024282006 — Class I MDR by ULMA Medical…

MD Atlas
ULMA Medical Technologies, S.L.U.

EUDAMED last updated this device on Jul 28, 2023

08437024282006

8437024282ULMASWPLTGR01GD

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ULMA Medical Technologies, S.L.U.
UDI-DI code: 08437024282006
Reference / catalog number: 08437024282006

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Manufacturer information

Organization name: ULMA Medical Technologies, S.L.U.
SRN: ES-MF-000019352
Manufacturer status: Active

Market distribution

Primary placement in Spain; available across 3 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
France		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08437024282006
Basic UDI-DI: 8437024282ULMASWPLTGR01GD
Reference / catalog number: 08437024282006
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)

Z12129082VARIOUS OPHTALMOLOGY INSTRUMENTS - SOFTWARE ACCESSORIES
Z12040182GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES

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

084370242820138437024282ULMASWIAOFT016KOn 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.