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EUDAMED last updated this device on Jun 19, 2026
B-08806387823698Aurum Pro Absorbent Paper Points is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by META BIOMED CO., LTD.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
KR-MF-000009681KR19/81826259(01)08806387823698
1 warning recorded — scroll inside the panel to see all entries.
1. Should be use sterilized paper points 2. Do not use bent or broken points 3. Should be careful to avoid overfilling or dead space when applied sealer or cement 4. Use it immediately when applied sealer or cement 5. After using the paper points, should be kept in a cool place 6. Do not expose to direct sunlight 7. Do not reuse to prevent cross infections. (Secondary infections such as pathogens and viruses caused by saliva and blood)
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 Germany; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jun 25, 1998 | Still on market |
| EL | Jun 25, 1998 | Still on market |
| Spain | Jun 25, 1998 | Still on market |
| France | Jun 25, 1998 | Still on market |
| Italy | Jun 25, 1998 | Still on market |
| Netherlands | Jun 25, 1998 | Still on market |
| Portugal | Jun 25, 1998 | Still on market |
| Türkiye | Jun 25, 1998 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08806387823698Basic 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-08806387823698-UDI 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.
Q01010401PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRYPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Certificate health across this manufacturer's portfolio.
M.2025.MDR.1058AmendedHZ 2020208-1AmendedM.2025.MDR.1058-1WithdrawnNotified 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 →Notified 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 →Notified 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 →B-08806387823728On the marketAurum Pro Absorbent Paper PointsB-08806387823759On the marketAurum Pro Absorbent Paper PointsB-08806387823704On the marketAurum Pro Absorbent Paper PointsB-08806387823667On the marketAurum Pro Absorbent Paper PointsB-08806387823650On the marketAurum Pro Absorbent Paper PointsB-08806387823742On the marketNo certificate specifically references this device's Basic UDI-DI.