CDSCO UID MFG/MD/2019/000088_a7f379325518793f7cc92d63bcd401c0_ca7b2fbedf411af18de0e12aba2267b4

Angiography Guide Wire

Invent Biomed Private Limited·Device Class Class C·India CDSCO·Brand: MARATHON / MARATHONCTO+
Registration details
UID
MFG/MD/2019/000088_a7f379325518793f7cc92d63bcd401c0_ca7b2fbedf411af18de0e12aba2267b4
Device class
Class C
Brand name
MARATHON / MARATHONCTO+
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Guidewire is intended for percutaneous vessel entry using seldinger technique to facilitate the subsequent introduction of an intravascular device.
Similar products (3)
Other products with the same name or brand
Introducer Sheath
Brand: MARATHON / MARATHONCTO+
Invent Biomed Private Limited
Class C
Angiography guidewire
Brand: MARATHON / MARATHONCTO+
Invent Biomed Private Limited
Class C
PTCA Guidewire
Brand: MARATHON / MARATHONCTO+
Invent Biomed Private Limited
Class C
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
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
Angiography guidewire
Brand: MARATHON / MARATHONCTO+
Class C
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 Guide Wire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000088_a7f379325518793f7cc92d63bcd401c0_ca7b2fbedf411af18de0e12aba2267b4. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.