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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

FURADERM 30g — Class IIb MDR by Seid

MD Atlas
Seid

EUDAMED last updated this device on May 12, 2026

FURADERM 30g

8437013219cremaexternaCR

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Seid
UDI-DI code: 08470001934048
Reference / catalog number: 193404.8

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Manufacturer information

Organization name: Seid
SRN: ES-MF-000004010
Manufacturer status: Active

Related devices

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Critical warnings

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

CW999
Known hypersensitivity toany of the components of theproduct. Stop using the productin case of hypersensitivityreactions.

Market distribution

Primary placement in Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Jun 19, 2024	Still on market

Device identification

Trade name: FURADERM 30g
UDI-DI code: 08470001934048
Basic UDI-DI: 8437013219cremaexternaCR
Reference / catalog number: 193404.8
Issuing entity: GS1

Classification

Risk category: Class IIb
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)

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

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.