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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

T21475 — Class I 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

T21475

B-843655523214G6X3

On the marketClass I

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-843655523214G6X3
Reference / catalog number: T21475

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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

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

CW135
EUDAMED did not publish a description for this code.
CW011
External use. Avoid contact with eyes. In case of contact, rinse throughly with water. Avoid application on open wounds, intimate area, inside the mouth or into eyes, nose or ears.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	May 24, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-843655523214G6X3
Basic UDI-DI: B-843655523214G6X3
Reference / catalog number: T21475
Issuing entity: EUDAMED

Classification

Risk category: Class I
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)

M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)

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

HAMD1B-843655523217GCYAOn the market HAMD2B-843655523215G8XCOn the market HAMD6B-843655523221G3WMOn the market HAMD4B-843655523219GGYUOn the market HAMD5B-843655523220FZYROn 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.