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Apelem

FDA UDI

Class II (US FDA UDI)

by Apelem

Identity

Trade Name
APELEM FDA UDI
Generic Name
Basic diagnostic x-ray system table, powered FDA UDI
Device Name
Remote Controlled Radiology System FDA UDI
Model / Reference
FDX Visionary RF PREMIUM FDA UDI
Description
Remote Controlled Radiology System FDA UDI

Identifiers

Primary DI / UDI-DI
03760172650409 FDA UDI
510(k) Number
K203010 FDA UDI
FDA Product Code
JAA FDA UDI
GMDN Term
Basic diagnostic x-ray system table, powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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

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: Basic diagnostic x-ray system table, powered

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

Similar devices

Also classified as Basic diagnostic x-ray system table, powered.

Cleared under the same submission

K203010 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apelem

Sources (1)

  • FDA UDI 22c131e4-ca04-4f54-945d-047d64071910 34 fields · synced May 30, 2026