Henry Schein Maxima

Organization name

Henry Schein Inc.

SRN

US-MF-000021683

Manufacturer status

Active

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

Primary placement in Germany; available across 12 countries total.

Trade name

Henry Schein Maxima

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.

10304040103033

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.

B-10304040103033

Reference / catalog number

5701229

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 I

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

Maxima sterile K File 21 mm #90

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

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

• L159004ENDODONTIC RASPS AND FILES, REUSABLE

• Class I medical devices in EUDAMED