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priti®multidisc ZrO2

FDA UDI

Class II (US FDA UDI)

by Pritidenta GmbH

Identity

Trade Name
priti®multidisc ZrO2 FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Model / Reference
13107-D985-10C4HT FDA UDI

Identifiers

Primary DI / UDI-DI
04251366900695 FDA UDI
510(k) Number
K161025 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, ceramic

priti®multidisc ZrO2 by Pritidenta GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pritidenta GmbH

Sources (1)

  • FDA UDI f18e060a-6c42-43db-878f-73539e31c77e 33 fields · synced Jun 8, 2026