← Back to catalogue

Vertex-Dental BV

FDA UDI

Class I (US FDA UDI)

by Vertex-Dental B.V.

Identity

Trade Name
Vertex-Dental BV FDA UDI
Generic Name
Dental prosthesis bite verification device FDA UDI
Device Name
3D printing material for try-in devices FDA UDI
Model / Reference
NDTRPI01000 FDA UDI
Description
3D printing material for try-in devices FDA UDI

Identifiers

Primary DI / UDI-DI
08719425508658 FDA UDI
FDA Product Code
EEA FDA UDI
GMDN Term
Dental prosthesis bite verification device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6200 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Dental prosthesis bite verification device

Vertex-Dental BV by Vertex-Dental B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis bite verification device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Vertex-Dental B.V.

Sources (1)

  • FDA UDI dd01fffb-ddac-464d-b975-bd2f1330afb6 33 fields · synced May 30, 2026