- Role
- Country
- Date of registration
- Address
LI-MF-000000522No 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.IPS e.max Ceram Glaze Paste FLUO 3 g is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Ivoclar Vivadent AG. Placed on the EU market in Liechtenstein. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 11, 2026
76152082ACERA008F6Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)07615208379686
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.
07615208379686Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
76152082ACERA008F6597042UDI 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.
1 packaging level registered — each level carries its own UDI-DI.
07615208379686× 1 unitBase unit07615208449266× 10 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER76152082AACCE0058TOn the marketIPS e.max Ceram Gl-Stain Liq.15 ml long76152082AACCE0058TOn the marketIPS e.max Ceram Glaze Paste 3 g76152082ACERA008F6On the marketIPS e.max Ceram Glaze Powder 5 g76152082ACERA008F6On the marketIPS e.max Ceram Glaze Powder FLUO 5 g76152082ACERA008F6On the marketIPS e.max Ceram Glaze Spray 120 ml76152082ACERA008F6On the marketNo certificate specifically references this device's Basic UDI-DI.