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EUDAMED last updated this device on Jun 12, 2026
87179737120YQSerological Pipette 10 mL is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by BIRR Biosciences BV. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
087179737145691137101 packaging level registered — each level carries its own UDI-DI.
08717973714569× 1 unitBase unit08717973712633× 500 unitsNL-MF-000023194(01)08717973714569
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Belgium; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Mar 31, 2025 | Still on market |
| Germany | Mar 31, 2025 | Still on market |
| Denmark | Mar 31, 2025 | Still on market |
| EL | Mar 31, 2025 | Still on market |
| Spain | Mar 31, 2025 | Still on market |
| France | Mar 31, 2025 | Still on market |
| Hungary | Mar 31, 2025 | Still on market |
| Ireland | Mar 31, 2025 | Still on market |
| Netherlands | Mar 31, 2025 | Still on market |
| Romania | Mar 31, 2025 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
U080299DEVICES FOR ASSISTED REPRODUCTION - OTHERPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →87179737110YMOn the marketSemen Collection Container 100 mL87179737110YMOn the marketSerological Pipette 1 mL87179737120YQOn the marketSerological Pipette 25 mL87179737120YQOn the marketSerological Pipette 2mL87179737120YQOn the marketSerological Pipette 5 mL87179737120YQOn the marketCertificate health across this manufacturer's portfolio.
BE25/00000073RestrictedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →