Maude adverse event report: arjohuntleigh magog inc. Maxi sky 2 manufactured ceiling fixed cassette. May 15, 2013 Transferring from a bed to a chair featuring the Application of a Universal Sling and A 150F Folding - Duration: 2:41. Prism Medical UK 48,742 views. Hamilton beach coffee maker instructions pdf.
Equipment layout. It is recommended to request site-specific drawings from a Philips representative early in the design process. Brilliance CT 64-channel Equipment Layout Recommended Ceiling Height: 9'-0' (2743mm) Minimum Ceiling Height: 8'-0' (2440mm). Philips ct brilliance 64 user manual pdf.
-
| 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 |
|
Arjo Maxi Sky 2
| ARJOHUNTLEIGH MAGOG INC. MAXI SKY 2 MANUFACTURED CEILING FIXED CASSETTE | Back to Search Results |
| | Model Number MS000-01-01 | | Device Problem Appropriate Term/Code Not Available | | Event Date 11/03/2012 | | Event Type Malfunction | | Event Description | While getting a pt up to the chair with a ceiling lift and a loop sling, the right leg loop of the sling unhooked from the spreader bar, causing the pt's leg to drop. This happened when the pt was raised from the bed, so no injuries were sustained. | | Manufacturer Narrative | Logitech harmony 520 user manual. This report is being filed under exemption (b)(4) by arjohuntleigh on behalf of the mfr arjohuntleigh (b)(4). Download pci compliance full manual example. Add'l info will be provided following the conclusion of the mfr's investigation. | | Search Alerts/Recalls |
|
|
Arjo Maxi Sky 2 Manual
| New Search | Submit an Adverse Event Report |
Arjohuntleigh Maxi Sky 2 Service Manual
Arjo Maxi Sky 2 Service Manual
| Type of Device | MANUFACTURED CEILING FIXED CASSETTE |
|---|
| Manufacturer (Section D) | | ARJOHUNTLEIGH MAGOG INC. | | 2001 tanguay st. | | magog, quebec J1X 5Y5 | | CA J1X 5Y5 |
|
|---|
| Manufacturer (Section G) | | ARJOHUNTLEIGH MAGOG INC. | | 2001 tanguay st. | | magog, quebec J1X 5Y5 | | CA J1X 5Y5 |
|
|---|
| Manufacturer Contact | | steve kahn | | 2349 west lake st. | | addison , IL 60101 | | 8003231245 |
|
|---|
| MDR Report Key | 2862281 |
|---|
| Report Number | 9681684-2012-00097 |
|---|
| Device Sequence Number | 1 |
|---|
| Product Code | FNG |
|---|
| Report Source | Manufacturer |
|---|
| Source Type | User facility |
|---|
| Reporter Occupation |
|---|
| Type of Report | Initial |
|---|
| Report Date | 11/28/2012,11/05/2012 |
|---|
| 1 Device Was Involved in the Event |
|---|
| 0 PatientS WERE Involved in the Event: |
|---|
| Date FDA Received | 11/29/2012 |
|---|
| Is This An Adverse Event Report? | No |
|---|
| Is This A Product Problem Report? | Yes |
|---|
| Device Operator | HEALTH PROFESSIONAL |
|---|
| Device MODEL Number | MS000-01-01 |
|---|
| Was Device Available For Evaluation? | Yes |
|---|
| Was the Report Sent to FDA? | Yes |
|---|
| Date Report Sent to FDA | 11/28/2012 |
|---|
| Distributor Facility Aware Date | 11/05/2012 |
|---|
| Date Report TO Manufacturer | 11/28/2012 |
|---|
| Date Manufacturer Received | 11/05/2012 |
|---|
| Was Device Evaluated By Manufacturer? | Device Not Returned To Manufacturer |
|---|
| Date Device Manufactured | 06/01/2012 |
|---|
| Is The Device Single Use? | No |
|---|
| Is this a Reprocessed and Reused Single-Use Device? | No |
|---|
| Type of Device Usage | Reuse |
|---|
|
|