Root elevator PREMIUM Bernard, fig. 2, left

Organization name

Fabryka Narzędzi Medycznych Chirmed Marcin Dyner Spółka Komandytowa

SRN

PL-MF-000052302

Manufacturer status

Active

1 warning recorded — scroll inside the panel to see all entries.

• CW129

  Products made of stainless steel contain metals (in the form of alloying additives or in trace amounts) that may cause allergies (Nickel, Chromium, Cobalt). The product is contraindicated for people with allergies to any component of steel.

Primary placement in Poland; available across 32 countries total.

Trade name

Root elevator PREMIUM Bernard, fig. 2, left

UDI-DI code

05904151420197

Basic UDI-DI

B-05904151420197

Reference / catalog number

ST 4023

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

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.

• L159002DENTAL EXCAVATORS, REUSABLE