Devices

Device Recall Intubation Flexible Fiberscope

Model / Serial
C1140, C1140E, C1160, C1160E, QKC1750, QKC1750E, QKC1694, QKC1694E
Product Classification
Anesthesiology Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
Intubation Flexible Fiberscope, Models: 11301AA1, 11301BN1, 11302BD1, 11302BD2, 11304BC1, 11340BC1, 11301BND1, 11302BDD1, and 11302BDD2. || " Transoral intubation " Transnasal intubation " Evaluation of placement of endotracheal and double lumen endotracheal tubes " Provide visual access to the larynx and tracheobronchial tree.
Manufacturer
Karl Storz Endoscopy America Inc
1 Event
- Recall of Device Recall Intubation Flexible Fiberscope

Manufacturer

Karl Storz Endoscopy America Inc

Manufacturer Address
Karl Storz Endoscopy America Inc, 15 Wells St, Southbridge MA 01550-4503
Manufacturer Parent Company (2017)
Karl Storz SE & Co. KG
Source
USFDA

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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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