- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Oct 23, 2025
B-07895742285999Conventional bracket archwire sequence - 18 Arcs is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by DENTAL MORELLI LTDA.. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0789574228599950.14.900(01)07895742285999
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q010405ORTHODONTIC WIRESBR-MF-000004812675541Primary placement in Portugal; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PortugalPrimary placement | — | Still on market |
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 →7895742133FZOn the marketContra Angle KeyB-07895742283162On the marketConventional bracket archwire sequence - 18 Arcs7895742172GBOn the marketDisposable Point for FinishingB-07895742246327On the marketDisposable Point for Finishing7895742181GCOn the marketDisposable Tray - Upper / Lower Pair - LB-07895742245566On the marketNo 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.No certificate specifically references this device's Basic UDI-DI.