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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

180 Rectangles de cotton 8X10cm — Class I MDR by HIDROFER SA

MD Atlas
HIDROFER SA

EUDAMED last updated this device on Mar 31, 2026

180 Rectangles de cotton 8X10cm

5607324REQUALGODHIDROFEN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: HIDROFER SA
UDI-DI code: 03664696003850
Reference / catalog number: 131429

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View device family (Basic UDI)

Manufacturer information

Organization name: HIDROFER SA
SRN: PT-MF-000002824
Manufacturer status: Active

Critical warnings

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

CW999
Tenir hors de portée des enfants.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: 180 Rectangles de cotton 8X10cm
UDI-DI code: 03664696003850
Basic UDI-DI: 5607324REQUALGODHIDROFEN
Reference / catalog number: 131429
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Doux & resistants; Haute Absorption; Blanchis sans Chlore; Coton sans pesticide.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 8 MU10
10 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M010101HYDROPHILIC COTTON

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

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Related devices

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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.