Organization name

Nobel Biocare AB

SRN

SE-MF-000000009

Manufacturer status

Active

No certificate specifically references this device's Basic UDI-DI.

3 warnings recorded — scroll inside the panel to see all entries.

• Do not use if package is damaged
• Consult instructions for use
• Caution

Primary placement in Sweden; available across 31 countries total.

Trade name

Drill Stop Ø3.8

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

07332747210231

Basic UDI-DI

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.

73327470000001226R

Reference / catalog number

33080

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

GS1

Risk category

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.

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://ifu.nobelbiocare.com/

Clinical sizes

• 3.8 MU50

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

European Medical Device Nomenclature — the EU product classification assigned to this device.

• L159099ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER

• Class IIa medical devices in EUDAMED