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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

9004782 — Class I MDR by LABORATORIOS HARTMANN…

MD Atlas
LABORATORIOS HARTMANN S.A.

EUDAMED last updated this device on May 13, 2026

9004782

84105581692QV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATORIOS HARTMANN S.A.
UDI-DI code: 08410558002753
Reference / catalog number: 9004782

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Manufacturer information

Organization name: LABORATORIOS HARTMANN S.A.
SRN: ES-MF-000002991
Manufacturer status: Active

Related devices

900698084105581692QVOn the market 900699084105581692QVOn the market 900697084105581692QVOn the market 900696184105581692QVOn the market 900694084105581685QYOn 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.

Critical warnings

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

CW009
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: 08410558002753
Basic UDI-DI: 84105581692QV
Reference / catalog number: 9004782
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: 2.5 MU10
5 MU36

EMDN nomenclature code(s)

M050199SURGICAL PLASTERS - 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
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Software identification