- Role
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- Date of registration
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EUDAMED last updated this device on Mar 11, 2026
76152082APROS004VZPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →SR Vivodent DCL Set of 6 UA56 A2 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.
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 →07615208400908Basic 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 →76152082APROS004VZ564898UDI 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 →(01)07615208400908
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHERSterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in Liechtenstein; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| LiechtensteinPrimary placement | Still on market |
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.76152082ABOND001HJOn the marketAdhese 2 100 Refill Bottle 1x6g76152082ABOND010HKOn the marketAdhese 2 Brush DC Endo blue 25 pcs76152082ABOND010HKOn the marketAdhese 2 Brush DC Reg. blue 25 pcs76152082ABOND010HKOn the marketAdhese 2 DC Ref. SD Sm/Endo 25x0.1g76152082ABOND010HKOn the market