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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

9308264 — Class I MDD by Lilleborg AS

MD Atlas
Lilleborg AS

EUDAMED last updated this device on Jun 10, 2025

9308264

B-07615400234943

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Lilleborg AS
UDI-DI code: 07615400234943
Reference / catalog number: 9308264

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View device family (Basic UDI)

Manufacturer information

Organization name: Lilleborg AS
SRN: NO-MF-000012956
Manufacturer status: Active

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Critical warnings

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

CW073
EUDAMED did not publish a description for this code.
CW084
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Norway; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 07615400234943
Basic UDI-DI: B-07615400234943
Reference / catalog number: 9308264
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Mildly alkaline cleaning product for machine washing of re-usable medical equipment and instruments in washer-disinfectors. Product is sold via retailers in 200 l drum (220 kg), and mainly within the Norwegian market (that is part of EU/EEA).
Additional information URL: https://products.solenis.com/no/product/dekoren-mild-3x55kg-L-7584
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)07615400234943

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EMDN nomenclature code(s)

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

V0799PRODUCTS FOR CLEANING MEDICAL DEVICES NOT INCLUDED IN OTHER CLASSES - 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

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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.