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Polystar Selection EDITION

FDA UDI

Class II (US FDA UDI)

by Merz Dental GmbH

Identity

Trade Name
Polystar Selection EDITION FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
posteriors; shade B2; size XL; lower jaw FDA UDI
Model / Reference
posteriors; shade B2; size XL; lower jaw FDA UDI
Description
posteriors; shade B2; size XL; lower jaw FDA UDI

Identifiers

Catalog Number
1982049 FDA UDI
Primary DI / UDI-DI
D7091982049 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resin artificial teeth

Polystar Selection EDITION by Merz Dental GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merz Dental GmbH

Sources (1)

  • FDA UDI e245c69a-a30b-4d44-9434-ed2e0c77e638 35 fields · synced Jun 1, 2026