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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

1020 — Class IIa MDD by Dörr Kampen B.V.

MD Atlas
Dörr Kampen B.V.

EUDAMED last updated this device on Jan 17, 2025

1020

B-08721249463020

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Dörr Kampen B.V.
UDI-DI code: 08721249463020
Reference / catalog number: 1020

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View device family (Basic UDI)

Manufacturer information

Organization name: Dörr Kampen B.V.
SRN: NL-MF-000000113
Manufacturer status: Active

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80.2008721249463MFJYOn the market 80.2808721249463MFJYOn the market 2020B-08721249463013On the market 4020B-08721249463006On the market 50148721249463VAKHOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08721249463020
Basic UDI-DI: B-08721249463020
Reference / catalog number: 1020
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: De Dörr Nova 1000 reinigt en desinfecteert bedpannen, urinalen, maatkannen en waskommen.
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)08721249463020

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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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