Devices

Device Recall Broncho Flexible Fiberscope

Model / Serial
C1140, C1140E, C1160, C1160E, QKC1750, QKC1750E, QKC1694, QKC1694E
Product Classification
Dental Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
Broncho Flexible Fiberscope, models: 11001BN1, 11002BD1, 11004BC1, and 11009BC1. || " Examination and treatment of the tracheobronchial tree Contraindications for Bronchoscopy " Uncontrolled angina, uncontrolled heart failure, or serious uncontrolled ventricular arrhythmias " Uncontrolled hypertension " Bleeding disorder or use of anticoagulants.
Manufacturer
Karl Storz Endoscopy America Inc
1 Event
- Recall of Device Recall Broncho 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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