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Vitallium ®

FDA UDI

Class II (US FDA UDI)

by DeguDent GmbH

Identity

Trade Name
Vitallium ® FDA UDI
Generic Name
Dental casting non-noble alloy FDA UDI
Model / Reference
Vitallium Laser Weld Wire .50 MM 2M Spools FDA UDI

Identifiers

Catalog Number
5535000180 FDA UDI
Primary DI / UDI-DI
EDD155350001800 FDA UDI
FDA Product Code
EJH FDA UDI
GMDN Term
Dental casting non-noble alloy FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3710 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

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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.5 Millimeter FDA UDI

Category: Dental casting non-noble alloy

Vitallium ® by DeguDent GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental casting non-noble alloy.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DeguDent GmbH

Sources (1)

  • FDA UDI f8a2b05e-1e0b-4095-b7b4-3ddd10eb7926 35 fields · synced Jun 8, 2026