• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PANORAMIC CORPORATION PANORAMIC X-RAY MODEL PC-1000

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

PANORAMIC CORPORATION PANORAMIC X-RAY MODEL PC-1000 Back to Search Results
Model Number 800724-1
Device Problems Migration or Expulsion of Device (1395); Unintended Movement (3026)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 11/14/2016
Event Type  malfunction  
Event Description
Received a email from a customer about their machine drifting down.The machine will keep drifting down once the height is set until it reaches the patient's shoulders.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
PANORAMIC X-RAY MODEL PC-1000
Type of Device
PC-1000
Manufacturer (Section D)
PANORAMIC CORPORATION
4321 goshen road
fort wayne IN 46818
Manufacturer (Section G)
PANORAMIC CORPORATION
4321 goshen road
fort wayne IN 46818
Manufacturer Contact
tammy shiffler
4321 goshen road
fort wayne, IN 46818
8006542027
MDR Report Key6157780
MDR Text Key61878478
Report Number1832462-2016-00020
Device Sequence Number1
Product Code EHD
UDI-Device Identifier00862309000309
UDI-Public00862309000309
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K870236
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer,health professional
Reporter Occupation Dentist
Type of Report Initial
Report Date 12/09/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/09/2016
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Dentist
Device Model Number800724-1
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Date Manufacturer Received11/14/2016
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured08/30/2000
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
-
-