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DE-MF-000009538CE 630493Angled Anatomic Abutment S 2mm 25 degree is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Bio3 Implants GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 25, 2026
B-04060475001052Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04060475001052
1 warning recorded — scroll inside the panel to see all entries.
CW007Sterile
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 Germany; available across 12 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Sep 10, 2015 | Dec 31, 2027 |
| Belgium | Dec 22, 2020 | Dec 31, 2027 |
| Cyprus | Aug 1, 2025 | Dec 31, 2027 |
| Czechia | Dec 22, 2020 | Dec 31, 2027 |
| Denmark | Dec 22, 2020 | Dec 31, 2027 |
| EL | Dec 22, 2020 | Dec 31, 2027 |
| Spain | Dec 22, 2020 | Dec 31, 2027 |
| France | Dec 22, 2020 | Dec 31, 2027 |
| Netherlands | Dec 22, 2020 | Dec 31, 2027 |
| Poland | Dec 22, 2020 | Dec 31, 2027 |
| Romania | Dec 22, 2020 | Dec 31, 2027 |
| Türkiye | — | Dec 31, 2027 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
04060475001052Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-04060475001052EAAS2502UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
P01020180DENTAL IMPLANTS - ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
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.B-04060475001021On the marketAngled Anatomic Abutment S 15 degree 3mmB-04060475001038On the marketAngled Anatomic Abutment S 25 degreeB-04060475001045On the marketAngled Anatomic Abutment W. 15 degreeB-04060475001069On the marketAngled Anatomic Abutment W. 15 degree 1mmB-04060475001076On the marketAngled Anatomic Abutment W. 15 degree 2mmB-04060475001083On the market