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Retrievable Vena Cava Filter and Introduction Kit - India CDSCO Medical Device Registration

Retrievable Vena Cava Filter and Introduction Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000147_83fd13ec70b3e6c4563942d5d17e5eda_d2db9efbc4863680b9e8d58d44826af6. This device is marketed under the brand name OPTEASE®. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO.

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CDSCO Registered
Class Class D
Retrievable Vena Cava Filter and Introduction Kit
UID: IMP/MD/2022/000147_83fd13ec70b3e6c4563942d5d17e5eda_d2db9efbc4863680b9e8d58d44826af6

Brand Name

OPTEASE®

Device Class

Class D

Approving Authority

CDSCO

Product Information

The OPTEASE Retrievable Vena Cava Filter is indicated for the prevention of pulmonary embolism (OPTEASE®) via percutaneous placement in the IVC in patients considered at high risk of PE. The Angiographic Vessel Dilator is designed to provide angiographic visualization and linear measurement of the vasculature when combined with the delivery of radiopaque contrast media to the vena cava.

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