CDSCO UID MFG/MD/2022/000128_23d0a90a85a6670ac1e8fd79d51a7829_88c70358c6ce7c26c25fcc4b8615ceca

PTCA guidewire

Suretech Medical Inc·Device Class Class D·India CDSCO·Brand: SURETECH
Registration details
UID
MFG/MD/2022/000128_23d0a90a85a6670ac1e8fd79d51a7829_88c70358c6ce7c26c25fcc4b8615ceca
Device class
Class D
Brand name
SURETECH
License holder
Suretech Medical Inc
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
Intended for use in interventional cardiology procedures
Similar products (10)
Other products with the same name or brand
CVC Catheter KIT
Brand: SURETECH
Suretech Medical Inc
Class C
GUIDEWIRE
Brand: SURETECH
Suretech Medical Inc
Class D
INTRODUCER SHEATH
Brand: SURETECH
Suretech Medical Inc
Class C
PTCA Balloon catheter
Brand: SURETECH
Suretech Medical Inc
Class B
RADIAL COMPRESSION BAND
Brand: SURETECH
Suretech Medical Inc
Class B
FISTULA NEEDLE
Brand: SURETECH
Suretech Medical Inc
Class B
ASPIRATION CATHETER
Brand: SURETECH
Suretech Medical Inc
Class B
PUNCTURE SHEATH
Brand: SURETECH
Suretech Medical Inc
Class B
DILATORS
Brand: SURETECH
Suretech Medical Inc
Class B
MALECOT / SUPRAPUBIC CATHETER WITH NEEDLE
Brand: SURETECH
Suretech Medical Inc
Class B
Other products from Suretech Medical Inc
Products from the same license holder (10 products)
CVC Catheter KIT
Brand: SURETECH
Class C
GUIDEWIRE
Brand: SURETECH
Class D
INTRODUCER SHEATH
Brand: SURETECH
Class C
PTCA Balloon catheter
Brand: SURETECH
Class B
RADIAL COMPRESSION BAND
Brand: SURETECH
Class B
FISTULA NEEDLE
Brand: SURETECH
Class B
ASPIRATION CATHETER
Brand: SURETECH
Class B
PUNCTURE SHEATH
Brand: SURETECH
Class B
Pacing electrode
Class B
DILATORS
Brand: SURETECH
Class B
About this record

PTCA guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000128_23d0a90a85a6670ac1e8fd79d51a7829_88c70358c6ce7c26c25fcc4b8615ceca. This device is marketed under the brand name SURETECH. The license holder is Suretech Medical Inc, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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