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Organization name
UDI-DI code
Reference / catalog number

690032562 — Class IIa MDD by ISDIN, S.A

MD Atlas
ISDIN, S.A

EUDAMED last updated this device on Jan 14, 2026

690032562

B-4600569Y3

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ISDIN, S.A
UDI-DI code: D-4600569Y3
Reference / catalog number: 690032562

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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
Warnings: non-hormonal treatment. WOMAN ISDIN® Lubricant can be used together with hormone replacement therapy. Ask your doctor if you are using another vaginal treatment: its interaction with other treatments has not been tested. Do not apply on wounds. Do not ingest. Do not use it in case of allergy to any component of WOMAN ISDIN® Lubricant. If you have an adverse reaction, discontinue use and consult your doctor. Indicated in women from fertile age to post menopause. Avoid contact with eyes. Keep out of reach of children.

Market distribution

Primary placement in Spain; available across 2 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Portugal		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-4600569Y3
Basic UDI-DI: B-4600569Y3
Reference / catalog number: 690032562
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
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)

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

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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.