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Planmed

FDA UDI

Class II (US FDA UDI)

by Planmed Oy

Identity

Trade Name
Planmed FDA UDI
Generic Name
Limited-view-field CT system FDA UDI
Device Name
Planmed Verity is a CBCT x-ray scanner for the diagnosis of extremities and the head. FDA UDI
Model / Reference
Verity FDA UDI
Description
Planmed Verity is a CBCT x-ray scanner for the diagnosis of extremities and the head. FDA UDI

Identifiers

Primary DI / UDI-DI
06430035430062 FDA UDI
FDA Product Code
OAS FDA UDI
JAK FDA UDI
GMDN Term
Limited-view-field CT system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Limited-view-field CT system

Planmed by Planmed Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limited-view-field CT system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Planmed Oy

Sources (1)

  • FDA UDI 4cb15f59-6673-4e6d-b371-5600c9a85f51 33 fields · synced Jun 6, 2026