International Medical Devices Database

Manufacturer Address
LMA North America Inc, 4660 La Jolla Village Dr Ste 900, San Diego CA 92122-4608
Manufacturer Parent Company (2017)
Lma North America, Incorporated
Source
USFDA
1 Event
- Recall of Device Recall LMA Esophageal Intubation Detector (EID), Catalog Number EID100

One device in the database

Device Recall LMA Esophageal Intubation Detector (EID), Catalog Number EID100

Model / Serial
2009 Lot # 90923A, 91222A. 2010 Lot# 00327A, 00518A, 00623A, 00831B, 01013A, 01103A, 01214A. 2011 Lot# 10110A, 10301B, 10423A, 10530A, 10602A, 10703A, 10804A, 11004A. 2012 Lot# 120104, 120414.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution--USA (nationwide) and the countries of Canada, United Kingdom, ZA, and Australia.
Product Description
LMA Esophageal Intubation Detector (EID), Catalog Number EID100 || The device is used to assist verification of placement of the endotracheal tube or esophageal/tracheal double lumen tube. This device is to be used as an adjunct to assess intubation. Its purpose is not to eliminate clinical judgment

One manufacturer with a similar name

Learn more about the data here

LMA North America Inc

Manufacturer Address
LMA North America Inc, 9360 Towne Centre Dr, San Diego CA 921213030
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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