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CediTEC DB

FDA UDI

Class II (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
CediTEC DB FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
Disc orange-pink 30 mm FDA UDI
Model / Reference
6197 FDA UDI
Description
Disc orange-pink 30 mm FDA UDI

Identifiers

Catalog Number
6197 FDA UDI
Primary DI / UDI-DI
E2216197 FDA UDI
FDA Product Code
EBI FDA UDI
MQC FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
Not 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

CediTEC DB by VOCO GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (1)

  • FDA UDI 06da4d7e-9c87-4a27-93b4-958229058f88 37 fields · synced Jun 8, 2026