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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

2295796FG — Class IIb MDD by Soluscope SAS

MD Atlas
Soluscope SAS

EUDAMED last updated this device on Apr 13, 2026

2295796FG

B-03597610439162

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Soluscope SAS
UDI-DI code: 03597610439162
Reference / catalog number: 2295796FG

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Manufacturer information

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

Critical warnings

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

CW070
EUDAMED did not publish a description for this code.
CW076
EUDAMED did not publish a description for this code.
CW081
EUDAMED did not publish a description for this code.
CW104
EUDAMED did not publish a description for this code.
CW139
EUDAMED did not publish a description for this code.
CW141
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW166
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW177
EUDAMED did not publish a description for this code.
CW430
EUDAMED did not publish a description for this code.
CW444
EUDAMED did not publish a description for this code.
CW179
EUDAMED did not publish a description for this code.
CW416
EUDAMED did not publish a description for this code.
CW397
EUDAMED did not publish a description for this code.
CW073
EUDAMED did not publish a description for this code.
CW080
EUDAMED did not publish a description for this code.
CW088
EUDAMED did not publish a description for this code.
CW119
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
XI	Jul 26, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03597610439162
Basic UDI-DI: B-03597610439162
Reference / catalog number: 2295796FG
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

SC8L-2D-A359761SS01561QEQBTOn the market SC8L-1D-C359761SS01561QEQBTOn the market SC8-2D-C359761SS01561QEQBTOn the market SC8-1D-C359761SS01561QEQBTOn the market SC8L-2D-C359761SS01561QEQBTOn the market

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.