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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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Dörr Nova 1000 — 1 UDI-DI variant, MDD (Dörr Kampen B.V.)

MD Atlas
Dörr Kampen B.V.

Data from EUDAMED, last updated May 30, 2026

Dörr Nova 1000

B-08721249463020

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Dörr Kampen B.V.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2121250CE01
Type: refdata.legacy.mdd-certificate-type.v
Notified body: DEKRA Certification B.V. (0344)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-08721249463020
Device name: —
Device model: Dörr Nova 1000
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jan 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: Dörr Kampen B.V.
SRN: NL-MF-000000113
Country: Netherlands
Email: info@dorrkampen.nl
Phone: +31 38 331 42 00

Variants by status

UDI-DI variants

1 UDI-DI variant

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Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

102008721249463020