Sterile UDG-Flash

Trade name

Sterile UDG-Flash

UDI-DI code

06942135226051

Basic UDI-DI

697312285UDGSRCF003L4

Reference / catalog number

SUFLA004031045

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

30

Additional product description

Sterile Root canal file is used with active instruments designed to cut, flatten, clean and shape teeth and root canals in dental root cana treatment. it contacts dentin or tissue for less than 24 hours. The device is sterile, single patient and procedure use.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

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

• Q010507ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE

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

• CW011

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW009

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.

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