- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 12, 2026
76152082BABUT003JCIPS e.max Press HT A1 10 pcs is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Ivoclar Vivadent AG. Placed on the EU market in Liechtenstein. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
LI-MF-000000522Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
(01)07615208505993
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 Liechtenstein; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| LiechtensteinPrimary placement | — | 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.
07615208505993Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
76152082BABUT003JC764034UDI 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.
P01020101DENTAL IMPLANTSCertificate health across this manufacturer's portfolio.
G15 043306 0282SupplementedNotified 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 →76152082BABUT003JCOn the marketIPS e.max Press HO 2 5 pcs76152082BABUT003JCOn the marketIPS e.max Press HO 2 L/3 pcs76152082BABUT003JCOn the marketIPS e.max Press HT A1 5 pcs76152082BABUT003JCOn the marketIPS e.max Press HT A1 5 pcs76152082BABUT003JCOn the marketIPS e.max Press HT A1 L/3 pcs76152082BABUT003JCOn the market