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14X17 Portable GOS Flat Panel Detector without USB

FDA UDI

Class II (US FDA UDI)

by Konica Minolta Medical Imaging U.s.a., Inc.

Identity

Trade Name
14X17 Portable GOS Flat Panel Detector without USB FDA UDI
Generic Name
Diagnostic x-ray digital imaging conversion system FDA UDI
Device Name
IR 14X17 Portable GOS Flat Panel Detector without USB (-R or -L) FDA UDI
Model / Reference
PAN241 FDA UDI
Description
IR 14X17 Portable GOS Flat Panel Detector without USB (-R or -L) FDA UDI

Identifiers

Primary DI / UDI-DI
00817100020247 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Diagnostic x-ray digital imaging conversion system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

No

FDA UDI

Category: Diagnostic x-ray digital imaging conversion system

14X17 Portable GOS Flat Panel Detector without USB by Konica Minolta Medical Imaging U.s.a., Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Diagnostic x-ray digital imaging conversion system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Konica Minolta Medical Imaging U.s.a., Inc.

Sources (1)

  • FDA UDI eaf08771-e5c8-4e60-bb98-1cad39d118f4 35 fields · synced May 30, 2026