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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

HAMD3 — Class III MDD by Instituto de…

MD Atlas
Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.

EUDAMED last updated this device on Feb 18, 2026

HAMD3

B-843655523218GEYK

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.
UDI-DI code: D-843655523218GEYK
Reference / catalog number: HAMD3

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Manufacturer information

Organization name: Instituto de Investigación Biotecnológica, Farmacéutica y Medicamentos Huérfanos, S.L.
SRN: ES-MF-000001065
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW011
Professional use
CW010
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW007
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	May 18, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-843655523218GEYK
Basic UDI-DI: B-843655523218GEYK
Reference / catalog number: HAMD3
Issuing entity: EUDAMED

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC 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)

P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES

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

T21475B-843655523214G6X3On the market HAMD1B-843655523217GCYAOn the market HAMD2B-843655523215G8XCOn the market HAMD6B-843655523221G3WMOn the market HAMD4B-843655523219GGYUOn 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.