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myQuickmat Prime kit

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6890

by Polydentia SA

Identity

Trade Name
myQuickmat Prime kit EUDAMEDFDA UDI
Generic Name
Dental matrix band kit FDA UDI
Device Name
myQuickmat Prime kit EUDAMED
Model / Reference
6890 EUDAMEDFDA UDI

Identifiers

Catalog Number
6890 FDA UDI
Primary DI / UDI-DI
+E29968900 EUDAMED
E29968900 FDA UDI
Basic UDI-DI
++E299PRIMEKITKH EUDAMED
FDA Product Code
DZN FDA UDI
EMDN Code
Q01010401 PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY EUDAMED
GMDN Term
Dental matrix band kit FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Medical Purpose
Sectional matrix system EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

myQuickmat Prime kit by Polydentia SA — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Polydentia SA
EUDAMED SRN
CH-PR-000009114

Sources (2)

  • EUDAMED 1a6e57dd-e236-478c-9e73-96c5aeafdb1d 61 fields · synced May 31, 2026
  • FDA UDI 80870eb6-a720-47ec-ab33-13e34e4553c5 33 fields · synced May 30, 2026