Desensibilize KF 2% (NORD)
Ref 4000021287
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number78996338DES002X8 07899633820634 | Date15 Sep 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Desensibilize KF
- Model / reference
- 4000021287
- Primary DI / UDI-DI
- 07899633820634
- Basic UDI-DI
- 78996338DES002X8
- EMDN code
- Q019008 Dentinal desensitisers
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Portugal
Manufacturer details
- EUDAMED SRN
- BR-MF-000004013
- Authorised representative
- Nuno Flores PT-AR-000003118
Other devices from Dentscare Ltda
Properties
Other properties (14)
- Supplied sterile: No
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No