MANIFOLD - India CDSCO Medical Device Registration
MANIFOLD is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000113_9dbaa6e6cafc0d78c8d831d11106f356_18f6e3017bb5b8bb818ae700c8dc6ba6. This device is marketed under the brand name SURETECH. The license holder is Suretech Medical Inc, and it is classified as Device Class Class B. The approving authority is Greater Mumbai Division.
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Brand Name
SURETECH
License Holder
Suretech Medical IncDevice Class
Approving Authority
Greater Mumbai Division
Product Information
INDICATED FOR FLUID FLOW DIRECTION CONTROL AND PROVIDING ACCESS PORT/PORTS FOR ADMINISTRATION OF A SOLUTION
CVC Catheter KIT
Brand: SURETECH
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GUIDEWIRE
Brand: SURETECH
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PTCA guidewire
Brand: SURETECH
Suretech Medical Inc
INTRODUCER SHEATH
Brand: SURETECH
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MANIFOLD
Brand: DELIVER
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MANIFOLD
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MANIFOLD
Brand: PROCONNKET
CARDIOMAC INDIA PRIVATE LIMITED
PTCA Balloon catheter
Brand: SURETECH
Suretech Medical Inc
RADIAL COMPRESSION BAND
Brand: SURETECH
Suretech Medical Inc
FISTULA NEEDLE
Brand: SURETECH
Suretech Medical Inc
CVC Catheter KIT
Brand: SURETECH
GUIDEWIRE
Brand: SURETECH
PTCA guidewire
Brand: SURETECH
INTRODUCER SHEATH
Brand: SURETECH
PTCA Balloon catheter
Brand: SURETECH
RADIAL COMPRESSION BAND
Brand: SURETECH
FISTULA NEEDLE
Brand: SURETECH
ASPIRATION CATHETER
Brand: SURETECH
PUNCTURE SHEATH
Brand: SURETECH

