IPS e.max Press MO 4 L/3 pcs

Organization name

Ivoclar Vivadent AG

SRN

LI-MF-000000522

Manufacturer status

Active

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

Primary placement in Liechtenstein; available across 1 country total.

Trade name

IPS e.max Press MO 4 L/3 pcs

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.

07615208381535

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.

76152082BABUT003JC

Reference / catalog number

596766

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 IIb

Applicable legislation

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

Status

On the market

Quantity

3

Additional product description

IPS e.max Press MO 4 L/3 pcs

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

1 packaging level registered — each level carries its own UDI-DI.

• 07615208381535× 1 unitBase unit
  • 07615208449433× 10 units

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

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

• P01020101DENTAL IMPLANTS

• Class IIb medical devices in EUDAMED

Certificate health across this manufacturer's portfolio.