- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 15, 2026
426066223CAPDHSLH DC Comfort Cap Ø 5.0 mm For Multi Unit Abutment is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by SLH Microtech GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04260662231259DC 32906DE-MF-000020864426066223BAP2On the marketSLH DC Cap for Universal Casting Abutment incl. ScrewB-04260662230214On the marketSLH DC Combining Screw for Multi Unit Abutment426066223SCQROn the marketSLH DC Cylinder Gingiva FormerB-04260662231488On the marketSLH DC Cylinder Gingiva FormerB-04260662231471On the marketSLH DC Cylinder Gingiva FormerB-04260662231495On the marketPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →2975-MED-2616701(01)04260662231259
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
CW010CW009Sterile
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 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jun 16, 2026 | Jun 15, 2031 |
| Türkiye | Jun 16, 2026 | Jun 15, 2031 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
P01020180DENTAL IMPLANTS - ACCESSORIESPrimary 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 →Certificate health across this manufacturer's portfolio.
2975-MED-2616701IssuedNotified 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.