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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

PHARAON980 — Class IIb MDD by LSO Medical

MD Atlas
LSO Medical

EUDAMED last updated this device on Mar 10, 2025

PHARAON980

B-03760227850310

On the marketClass IIb

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: LSO Medical
UDI-DI code: 03760227850310
Reference / catalog number: PHARAON980

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View device family (Basic UDI)

Manufacturer information

Organization name: LSO Medical
SRN: FR-MF-000009080
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW138
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jun 15, 2007	Dec 31, 2028

Device identification

Trade name: not provided
UDI-DI code: 03760227850310
Basic UDI-DI: B-03760227850310
Reference / catalog number: PHARAON980
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.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)03760227850310

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EMDN nomenclature code(s)

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

Z12011016DIODE SURGICAL LASER

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

ENDOV2B-03760227850365On the market PHARAON980B-03760227850020On the market ORLF000005_SBB-03760227850334On the market PHARAON1470B-03760227850013On the market ORLF000003_SBB-03760227850327On 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.