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EUDAMED last updated this device on Apr 13, 2022
00850024841DUSF108VGNL-MF-000011684Primary placement in Netherlands; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jul 27, 2012 | May 5, 2022 |
| Bulgaria | Jul 27, 2012 | May 5, 2022 |
| Cyprus | Jul 27, 2012 | May 5, 2022 |
| Czechia | Jul 27, 2012 | May 5, 2022 |
| Germany | Jul 27, 2012 | May 5, 2022 |
| Estonia | Jul 27, 2012 | May 5, 2022 |
| EL | Jul 27, 2012 | May 5, 2022 |
| Spain | Jul 27, 2012 | May 5, 2022 |
| France | Jul 27, 2012 | May 5, 2022 |
| Croatia | Jul 27, 2012 | May 5, 2022 |
| Italy | Jul 27, 2012 | May 5, 2022 |
| Lithuania | Jul 27, 2012 | May 5, 2022 |
| Luxembourg | Jul 27, 2012 | May 5, 2022 |
| Poland | Jul 27, 2012 | May 5, 2022 |
| Portugal | Jul 27, 2012 | May 5, 2022 |
| Romania | Jul 27, 2012 | May 5, 2022 |
| Slovenia | Jul 27, 2012 | May 5, 2022 |
| Slovakia | Jul 27, 2012 | May 5, 2022 |
(01)00850024841345
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W05020102SAMPLES TRANSPORT, BOXES0850024841BlueprintBBOn the marketMammaPrint BluePrint Breast Cancer Recurrence and Molecular Subtyping Kit085002484193128042On the marketNA (Centralized Lab Product)0850024841MammaprintK9On the marketDNS109.010850024841DNSZ3On the marketSpecimen Collection Kit0850024841ESM107QLOn the marketNo 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.