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Cercon®

FDA UDI

Class II (US FDA UDI)

by DeguDent GmbH

Identity

Trade Name
Cercon® FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Model / Reference
Cercon xt B2 disk 12 FDA UDI

Identifiers

Catalog Number
5366101612 FDA UDI
Primary DI / UDI-DI
EDD15366101612 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
Not 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 105 Millimeter FDA UDI

Cercon® by DeguDent 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
DeguDent GmbH

Sources (1)

  • FDA UDI a9cfaaae-8441-4ffe-b681-25c442443855 36 fields · synced Jun 6, 2026