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EUDAMED last updated this device on Jun 4, 2024
B-08800041355310IH Multi-unit Abutment Screw is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by SEWONMEDIX Inc.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08800041355310MAMSO200(01)08800041355310
European Medical Device Nomenclature — the EU product classification assigned to this device.
P01020101DENTAL IMPLANTS2 warnings recorded — scroll inside the panel to see all entries.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Mar 22, 2017 | Still on market |
KR-MF-000016194 KR19/81826295 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 →B-08800041354870On the marketIH Multi-unit AbutmentB-08800041354627On the marketIH Multi-unit Abutment ScrewB-08800041355358On the marketIH Multi-unit Abutment ScrewB-08800041355365On the marketIH Pick-up Impression Coping8800041300003014WOn the marketIH Pick-up Impression Coping8800041300003014WOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
HZ 2516998-1IssuedNotified 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.
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