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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

9006990 — Class I MDR by LABORATORIOS HARTMANN…

MD Atlas
LABORATORIOS HARTMANN S.A.

EUDAMED last updated this device on May 14, 2026

9006990

84105581692QV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATORIOS HARTMANN S.A.
UDI-DI code: 08470004534238
Reference / catalog number: 9006990

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Manufacturer information

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

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900698084105581692QVOn the market 900697084105581692QVOn the market 900696184105581692QVOn the market 900694084105581685QYOn the market 900695084105581685QYOn 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: 08470004534238
Basic UDI-DI: 84105581692QV
Reference / catalog number: 9006990
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: 1.25 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