← Back to catalogue

X-Ray Flat Panel Detector

FDA UDI

Class II (US FDA UDI)

by Canon Medical Systems Corporation

Identity

Trade Name
X-RAY FLAT PANEL DETECTOR FDA UDI
Generic Name
Indirect flat panel x-ray detector FDA UDI
Model / Reference
TFP-1216A FDA UDI

Identifiers

Primary DI / UDI-DI
04987670100345 FDA UDI
510(k) Number
K233107 FDA UDI
FDA Product Code
MQB FDA UDI
GMDN Term
Indirect flat panel x-ray detector 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

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

No

FDA UDI

Category: Indirect flat panel x-ray detector

X-Ray Flat Panel Detector by Canon Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indirect flat panel x-ray detector.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2a5fc07d-aa8c-4b7c-bd12-78e710649e41 33 fields · synced May 31, 2026