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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

Stérilux® ES — Class I MDR by Laboratoires PAUL…

MD Atlas
Laboratoires PAUL HARTMANN S.à.r.l

EUDAMED last updated this device on May 28, 2024

Stérilux® ES

32614810824C

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoires PAUL HARTMANN S.à.r.l
UDI-DI code: 03261480000233
Reference / catalog number: 241326

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Manufacturer information

Organization name: Laboratoires PAUL HARTMANN S.à.r.l
SRN: FR-MF-000004029
Manufacturer status: Active

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.

Critical warnings

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

CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

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: Stérilux® ES
UDI-DI code: 03261480000233
Basic UDI-DI: 32614810824C
Reference / catalog number: 241326
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: Compresses stériles 17 fils, 8 plis
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10 x 10 cm
10 x 10 cm

EMDN nomenclature code(s)

M020199COTTON GAUZES - 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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