006.012

Organization name

CeraRoot SL

SRN

ES-MF-000000251

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW999

  CeraRoot® Transporters must be used only by health professionals (dentists, doctors, or surgeons) that have received specific training and have advanced experience in oral surgery, periodontics, implantology, and prosthodontics.
• CW999

  For reprocessing CeraRoot® devices, always follow the instructions in the CeraRoot guideline EUD.008 - Reprocessing Instructions for Reusable surgical instruments and accessories.
• CW999

  Before use, the device must be carefully checked for proper function and damage.
• CW999

  Do not reuse if the product has signs of wear or damage.

Primary placement in Spain; available across 31 countries total.

Trade name

not provided

UDI-DI code

08435453900553

Basic UDI-DI

84354539CTEG

Reference / catalog number

006.012

Issuing entity

GS1

Risk category

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

Transporter 12 - ceramic for the CeraRoot® 12 dental implant.

Additional information URL

https://ifu.ceraroot.com/eifu

Clinical sizes

• Size for CeraRoot® 12 dental implant.

• P01020180DENTAL IMPLANTS - ACCESSORIES

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