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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

DIANA — Class I MDR by LID - SOTRAMET

MD Atlas
LID - SOTRAMET

EUDAMED last updated this device on Jan 23, 2024

DIANA

376036183DIANA7P

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LID - SOTRAMET
UDI-DI code: 03760361830490
Reference / catalog number: BOR51001B-ISC

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Manufacturer information

Organization name: LID - SOTRAMET
SRN: FR-MF-000014659
Manufacturer status: Active

Related devices

BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn the market BELLA376036183BELLA7NOn 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.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: DIANA
UDI-DI code: 03760361830490
Basic UDI-DI: 376036183DIANA7P
Reference / catalog number: BOR51001B-ISC
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: —
Additional information URL: https://medical.lid-lamps.com/en/produits/halogen-diana/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12010702MOBILE SCIALYTIC LAMPS

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

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