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EUDAMED last updated this device on Jun 24, 2026
880004925041BCDIO Fixture Driver assy (Machine) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by DIO Corporation. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08800049306352DIO Implant System Product Catalog Ver 7.0 (KR)(01)08800049306352
European Medical Device Nomenclature — the EU product classification assigned to this device.
P01020180DENTAL IMPLANTS - ACCESSORIESKR-MF-000008515The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Feb 11, 2026 | Still on market |
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.
View in glossary →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.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
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 →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 →880004926037BUOn the marketDIO Drill Extension Cover SET880004925041BCOn the marketDIO Fixture Driver assy (Machine)880004924023B3On the marketDIO Fixture Driver(Ratchet)880004921003A8On the marketDIO Fixture Driver(Ratchet)880004921003A8On the marketDIO Fixture Removing Driver880004921003A8On the marketCertificate health across this manufacturer's portfolio.
G15 068173 0026IssuedNotified 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.
No certificate specifically references this device's Basic UDI-DI.