Sedecal S.a.
PELAYA, 9 POL., ALGETE Madrid (Province), ES
Registered product codes
9 product codes
Recent MDR events
33 on file
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00001
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00002
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00003
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00008
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00009
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00004
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00007
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00005
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00006
- MOBILEDIAGNOST WDR 2.2Jun 23, 2023Injury3016618143-2023-00010
Recalls
4 on file
- TerminatedAug 14, 2015
Electrostatic energy may be stored in Systems that can cause a short-cicuit which, in turn, can generate an Electomagnetic Pulse which might disturb the electronics of the Digital Motion Control Board producing uncontrolled movements and such uncontrolled movements could cause the system to bump into the user or ppatient.
View FDA record ↗ - TerminatedFeb 2, 2015
Reports of unexpected movement.
View FDA record ↗ - Open, ClassifiedUnknown
A safety problem with installation and maintenance could lead to the breakage of the two steel cables that support the equipment to its roof anchor. Due to this, the equipment may fall and cause harm to the patient, user, or third parties.
View FDA record ↗ - TerminatedUnknown
This is related to previous 806 Notifications about uncommanded movements of a motorized mobile x-ray system. Reason for Recall: Along with the previously noted encoder and gauges problems and corresponding fixes, we have observed that static electricity can also elicit the unwanted behavior.
View FDA record ↗
Compliance history
Matched by FEI 3002495042.
FDA inspections
1 on file
- Official Action Indicated (OAI)Jan 24, 2025
Compliance: Devices · Citations posted
Inspection citations
4 on file
Top cited requirements
Compare to industry ↗- 21 CFR 803.17Jan 24, 2025
Lack of Written MDR Procedures
- 21 CFR 820.30(g)Jan 24, 2025
Design Validation - Risk analysis not performed/inadequate
- 21 CFR 820.100(a)Jan 24, 2025
Lack of or inadequate procedures
- 21 CFR 1010.2(c)Jan 24, 2025
Certification not based on adequate test/testing program
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.