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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

1242282 — Class IIb MDD by Soluscope SAS

MD Atlas
Soluscope SAS

EUDAMED last updated this device on Jun 17, 2025

1242282

B-03597610038532

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Soluscope SAS
UDI-DI code: 03597610038532
Reference / catalog number: 1242282

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Manufacturer information

Organization name: Soluscope SAS
SRN: FR-MF-000011763
Manufacturer status: Active

Critical warnings

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

CW058
EUDAMED did not publish a description for this code.
CW085
EUDAMED did not publish a description for this code.
CW091
EUDAMED did not publish a description for this code.
CW106
EUDAMED did not publish a description for this code.
CW139
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW166
EUDAMED did not publish a description for this code.
CW265
Contains Propan-2-ol.Dispose of the product and its container, following all precautions for use.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Mar 20, 2003	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03597610038532
Basic UDI-DI: B-03597610038532
Reference / catalog number: 1242282
Issuing entity: GS1

Classification

Risk category: Class IIb
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)

D050101PERACETIC AND ACETIC ACID WITH HYDROGEN PEROXIDE FOR THE DISINFECTION OF MEDICAL DEVICES

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

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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.