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Physioset TCR 6er

FDA UDI

Class II (US FDA UDI)

by Candulor AG

Identity

Trade Name
Physioset TCR 6er FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Model / Reference
552467 FDA UDI

Identifiers

Catalog Number
552467 FDA UDI
Primary DI / UDI-DI
E1995524671 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Resin artificial teeth

Physioset TCR 6er by Candulor AG — 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
Candulor AG

Sources (1)

  • FDA UDI 3ff3a642-ade6-48a4-af0b-f525419b2917 33 fields · synced Jun 8, 2026