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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

690029788 — Class IIa MDR by ISDIN, S.A

MD Atlas
ISDIN, S.A

EUDAMED last updated this device on Feb 2, 2026

690029788

8429420MDRTF0124P

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ISDIN, S.A
UDI-DI code: 08429420264595
Reference / catalog number: 690029788

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Manufacturer information

Organization name: ISDIN, S.A
SRN: ES-MF-000003221
Manufacturer status: Active

Critical warnings

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

CW999
Contra-indications: do not use if you are allergic or hypersensitive to any of the ingredients of the product. There is no data to support its use in pregnant women or children under 3 years of age. Consult your doctor with any questions. Warning: Keep this product out of reach of children. Do not apply to open wounds. Topical use. Do not ingest. To ensure the product is properly preserved, it is recommended to store it vertically, with the applicator brush facing upwards. In case of not noticing improvement or worsening, consult your doctor.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08429420264595
Basic UDI-DI: 8429420MDRTF0124P
Reference / catalog number: 690029788
Issuing entity: GS1

Classification

Risk category: Class IIa
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)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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
Serial number
Software identification

Related devices

ERYFOTONA AK-NMSC FLUIDB-ES-MF-0000032212GOn the market 6900297878429420MDRTF0124POn the market 6900263668429420MDRTF0124POn the market 6900227238429420MDRTF0124POn the market 6900263658429420MDRTF0124POn 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.