CANNEFF DNT GEL – DENTAL GEL

Organization name

CB21 Pharma, s.r.o.

SRN

CZ-MF-000037413

Manufacturer status

Active

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

• CW999

  Local irritation — redness, burning, or itching sensation at the application site, especially in patients with sensitive gums (probability: low, up to 1% of cases). Allergic reactions — manifested by swelling, redness, or rash (<0.1% of cases).

Primary placement in Czechia; available across 1 country total.

Trade name

CANNEFF DNT GEL – DENTAL GEL

UDI-DI code

8594197030411

Basic UDI-DI

859419703041DNT3P

Reference / catalog number

0001

Issuing entity

HIBCC

Risk category

Class IIa

Applicable legislation

MDR [Regulation (EU) 2017/745 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

8594197030411

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• V9017ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES

Certificate health across this manufacturer's portfolio.