Devices

Device Recall Airway stent

Model / Serial
OEM Catalog number 90129-212.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
Yes
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange 12x40 Airway Stent System; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 90129-212; || EXP (repackager), Aero (OEM) || Prosthesis, tracheal, expandable
Manufacturer
EXP Pharmaceutical Services Corp
1 Event
- Recall of Device Recall Airway stent

Manufacturer

EXP Pharmaceutical Services Corp

Manufacturer Address
EXP Pharmaceutical Services Corp, 48021Warm Springs Boulevard, Fremont CA 94539
Manufacturer Parent Company (2017)
Abry Partners Inc.
Source
USFDA

One device with a similar name

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Device Recall Airway stent

Model / Serial
OEM Catalog number 90129-209.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
Yes
Distribution
Distributed in DC and the states of CO, CA, FL, TX, and AR.
Product Description
Medical Device Exchange 10x40 Airway Stent System; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 90129-209; || EXP (repackager), Aero (OEM) || Prosthesis, tracheal, expandable
Manufacturer
EXP Pharmaceutical Services Corp

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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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