CDSCO UID MFG/MD/2019/000088_4d5bd38e09a362c518321e0d61811762_53657ee8be51c3317d86c3a7d2725534

Angiography guidewire

Invent Biomed Private Limited·Device Class Class C·India CDSCO·Brand: MARATHON / MARATHONCTO+
Registration details
UID
MFG/MD/2019/000088_4d5bd38e09a362c518321e0d61811762_53657ee8be51c3317d86c3a7d2725534
Device class
Class C
Brand name
MARATHON / MARATHONCTO+
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Guidewire is designed for percutaneous vessel entry using seldinger technique to facilitate the subsquent introduction of an intravascular device during invasive cardiology process
Similar products (3)
Other products with the same name or brand
Introducer Sheath
Brand: MARATHON / MARATHONCTO+
Invent Biomed Private Limited
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Angiography Guide Wire
Brand: MARATHON / MARATHONCTO+
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PTCA Guidewire
Brand: MARATHON / MARATHONCTO+
Invent Biomed Private Limited
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Other products from Invent Biomed Private Limited
Products from the same license holder (10 products)
Sirolimus Eluting Coronary Stent System
Brand: NOVA MATRIX®
Class D
Introducer Sheath
Brand: MARATHON / MARATHONCTO+
Class C
Angiography Guide Wire
Brand: MARATHON / MARATHONCTO+
Class C
Sirolimus Drug Eluting Coronary Stent System
Brand: NOVA MATRIX®
Class D
RAPID EXCHANGE PTCA DILATION CATHETER
Brand: NOVA MATRIX®
Class D
Co-Cr Stent Delivery System
Brand: NOVA MATRIX®
Class D
PTCA Guidewire
Brand: MARATHON / MARATHONCTO+
Class C
Rapid Exchange PTCA Post Dilation Catheter
Brand: NOVA MATRIX®
Class D
Trans Radial compression Device and Angio Closure Femo Seal Pad
Brand: COMPRESS TR / COMPRESS FC
Class A
PTCA Custom Kit
Brand: FLEXIPORT
Class B
About this record

Angiography guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000088_4d5bd38e09a362c518321e0d61811762_53657ee8be51c3317d86c3a7d2725534. This device is marketed under the brand name MARATHON / MARATHONCTO+. The license holder is Invent Biomed Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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