- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED data as of Jul 13, 2026
EUDAMED last updated this device on Aug 30, 2023
++B961DDPD2121KEBAYONET ROOTS ELEVATORS SET RIGHT is an EU MDR-regulated medical device on the European market. It is classified as Class I. Manufactured by Daddy D Pro. Placed on the EU market in Portugal. Explore certificates, regulatory status and the official record on MD Atlas.
B961DDPD21210DDP-D2-121B961DDPD21210
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q010399SURGICAL DENTAL DEVICES - OTHERPK-MF-000035172Primary placement in Portugal; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| PortugalPrimary placement | — | Still on market |
| Germany | — | Still on market |
| Spain | — | Still on market |
| Poland | — | 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.
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 DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
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.
UDI 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.
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
No certificate specifically references this device's Basic UDI-DI.
B-B961DP786044290On the marketBAYONET ROOTS ELEVATORS SET BAYONETBAYONET ROOTS ELEVATORS SET BAYONETBAYONET ROOTS ELEVATORS SET BAYONETBAYONET ROOTS ELEVATORS SET BAYONETBAYONET ROOTS ELEVATORS SET BAYONETBAYONET ROOTS ELEVATORS SET BAYONET++B961DDPD2122KGOn the marketBAYONET ROOTS ELEVATORS SET LEFT++B961DDPD2120KCOn the marketBAYONET ROOTS ELEVATORS SET STRAIGHT++B961DDPD2124KLOn the marketBAYONET ROOTS ELEVATORS SET WISDOM FOR 18 AND 38++B961DDPD2118KROn the marketBAYONET ROOTS ELEVATORS SET WISDOM FOR 28 AND 48B961DDPD21190++B961DDPD2119KTOn 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.