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CDSCO UID IMP/MD/2021/000368_41ced945bdff27f7f03329f1fe4f8266_ff81ada8815ac5f94fca60f2a1e81a07

Reinforced Endotracheal Tube

RESPICARE SOLUTIONS·Device Class Class B·India CDSCO·Brand: Respi-Evac
Registration details
UID
IMP/MD/2021/000368_41ced945bdff27f7f03329f1fe4f8266_ff81ada8815ac5f94fca60f2a1e81a07
Device class
Class B
Brand name
Respi-Evac
License holder
RESPICARE SOLUTIONS
Approving authority
CDSCO
Product information
Reinforced Endotracheal Tube, in combination with respiratory system, are intended for respiration during operation for patients who lose active breath ability.
Similar products (1)
Other products with the same name or brand
Endotracheal Tubes with Suction Lumen
Brand: Respi-Evac
RESPICARE SOLUTIONS
Class B
Other products from RESPICARE SOLUTIONS
Products from the same license holder (2 products)
Endotracheal Tubes with Suction Lumen
Brand: Respi-Evac
Class B
Nasal Oxygen Cannula
Brand: RAM Cannula
Class B
About this record

Reinforced Endotracheal Tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000368_41ced945bdff27f7f03329f1fe4f8266_ff81ada8815ac5f94fca60f2a1e81a07. This device is marketed under the brand name Respi-Evac. The license holder is RESPICARE SOLUTIONS, and it is classified as Device Class Class B. The approving authority is CDSCO.

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