- Mac User Forum
- Mcgrath Mac User Manual Free
- Mcgrath Mac User Manual Pdf
- Mcgrath Mac User Manual Free
- Mcgrath Mac User Manual
-
Refer to the McGRATH® MAC EMS Operator's Manual for complete directions for use, warnings and precautions. Refer to your organization’s protocols or policies regarding the use of the video laryngoscope. 60°C: Manual/machine cleaning and disinfection, sterilization with Steris ® AMSCO V-PRO 1, Sterrad (50S, 100S, 200, NX, 100NX) and EO gas. Detailed information on the validated methods and approved chemicals can be found in the in-depth instruction manual. McGRATH® MAC EMS Video Laryngoscope. It does not suggest protocols or policies regarding the use of the Video Laryngoscope. Refer to the Operating Instructions for complete directions for use, indications, contraindications, warnings, precautions and potential adverse events.
|
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO sterilized. Product Usage: Single Use, sterile video laryngoscope blade for use with McGRATH MAC Video Laryngoscopes. Setup Assistant helps you enter your Internet and email information and set up a user account on your iMac. If you already have a Mac, Setup Assistant can help you automatically transfer files, applications, and other information from your previous Mac to your new iMac. Page 13: More Information.
| |||||||||||||||||||||||||
Aircraft Medical Limited sent a recall notification letter dated November 4, 2014 to the sole US consignee. The letter included instructions for the consignee to: 1) check its own stock and its customers' stock for the recalled products; 2) arrange for any remaining stock to be removed from use. Customers with any questions can contact Aircraft Medical by e-mail at [email protected]. | |||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
40,900 blades (US); 16,000 blades (Foreign) | |||||||||||||||||||||||||
Worldwide Distribution - US Nationwide in the state of GA and the countries of Austria, China, Denmark, Finland, France, Hong Kong, Israel, Italy, Netherlands, Poland, Saudi Arabia, Singapore, South Korea, Taiwan, and Turkey. | |||||||||||||||||||||||||
TPLC Device Report | |||||||||||||||||||||||||
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. |