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Sirona Medical Radiology Platform

FDA UDI

Class I (US FDA UDI)

by Sirona Medical

Identity

Trade Name
Sirona Medical Radiology Platform FDA UDI
Generic Name
Radiology information system FDA UDI
Model / Reference
Model1 FDA UDI

Identifiers

Primary DI / UDI-DI
00860011175803 FDA UDI
FDA Product Code
LMD FDA UDI
GMDN Term
Radiology information system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.2020 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiology information system

Sirona Medical Radiology Platform by Sirona Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiology information system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sirona Medical

Sources (1)

  • FDA UDI 322d103c-bf4f-41ee-8c50-6be0c0036c17 32 fields · synced May 31, 2026