International Medical Devices Database

Manufacturer Address
Sechrist Industries Inc, 4225 E La Palma Ave, Anaheim CA 92807
Manufacturer Parent Company (2017)
Sechrist Industries Inc.
Source
USFDA
2 Events
- Recall of Device Recall Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module
- Recall of Device Recall Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module

2 devices in the database

Device Recall Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module

Model / Serial
Serial Numbers: 360001-360049, 360051-360064, 360068.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada
Product Description
Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3600E/ER || The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambient pressures

Device Recall Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module

Model / Serial
Serial Numbers: 330001-330069, 330071, 330072, 330074, 330075.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA (nationwide) and the countries of Bulgaria, and Canada
Product Description
Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER || The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambient pressures.

2 manufacturers with a similar name

Learn more about the data here

Sechrist Industries Inc

Manufacturer Address
Sechrist Industries Inc, 4225 E La Palma Ave, Anaheim CA 92807-1815
Manufacturer Parent Company (2017)
Sechrist Industries Inc.
Source
USFDA

SECHRIST INDUSTRIES INC.

Manufacturer Address
ANAHEIM
Manufacturer Parent Company (2017)
Sechrist Industries Inc.
Source
HC

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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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