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RFD Reference Detector

FDA UDI

Class II (US FDA UDI)

by IBA Dosimetry GmbH

Identity

Trade Name
RFD Reference Detector FDA UDI
Generic Name
Radiation electrometer FDA UDI
Device Name
RFD 3G-pSi Reference Detector, TNC FDA UDI
Model / Reference
999-802-T FDA UDI
Description
RFD 3G-pSi Reference Detector, TNC FDA UDI

Identifiers

Primary DI / UDI-DI
EIBA999802T0 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiation electrometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 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: Radiation electrometer

RFD Reference Detector by IBA Dosimetry GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation electrometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
IBA Dosimetry GmbH

Sources (1)

  • FDA UDI 5f535673-7055-4838-b295-50f6fb48b46a 34 fields · synced Jun 8, 2026