UDI-DI variants

18 UDI-DI variants

DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE Enamel04260296271102
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A104260296270969
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A2O04260296271065
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A304260296270983
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A3.504260296270990
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A3O04260296271072
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE A404260296270082
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE B104260296271003
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE B204260296271010
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE B304260296271027
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE C204260296271034
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE C304260296271041
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE D304260296271058
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE Insizal04260296271089
DYNAMIC PLUS REFILL SYRINGE - Light Cure Micro Hybrid Composite SHADE Pedo04260296271096
DYNAMIC PLUS REFILL SYRINGE- Light Cure Micro Hybrid Composite SHADE A204260296270976
DYNAMIC PLUS STANDARD KIT - Light Cure Micro Hybrid Composite 8 x 4 gr syringes04260296270952
DYNAMIC PLUS STARTER KIT - Light Cure Micro Hybrid Composite 5 x 4 gr syringes04260296270945

Data from EUDAMED, last updated May 23, 2026

DYNAMIC PLUS

426029627COM0053G

18 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: President Dental GmbH

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 426029627COM0053G
Device name: DYNAMIC PLUS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: President Dental GmbH
SRN: DE-MF-000014901
Country: Germany
Email: info@presidentdental.com
Phone: +49 8166 3899820

Variants by status

UDI-DI variants

18 UDI-DI variants