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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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CANNEFF DNT GEL - DENTAL GEL — 1 UDI-DI variant, MDR

MD Atlas
CB21 Pharma, s.r.o.

Data from EUDAMED, last updated May 31, 2026

CANNEFF DNT GEL - DENTAL GEL

859419703041DNT3P

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: CB21 Pharma, s.r.o.

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 2025-MDR/QS-032
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Jun 12, 2025 → Jun 12, 2030

Identity & classification

Basic UDI-DI: 859419703041DNT3P
Device name: CANNEFF DNT GEL - DENTAL GEL
Device model: CANNEFF DNT GEL - DENTAL GEL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: CB21 Pharma, s.r.o.
SRN: CZ-MF-000037413
Country: Czechia
Email: antonin.malik@cb21pharma.com
Phone: +420732302601

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQWC9JG11HZENQWKBKMFFQ0Z

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

CANNEFF DNT GEL – DENTAL GEL8594197030411