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CDSCO UID MFG/MD/2021/000346_aa06224a93603254ed27e23dc93903e5_fbfb3c75aa9abfd9ec2e56eb16cbc67a

Oxidized Regenerated Cellulose Haemostat

M/s. Universal ISO-MED (A Div. of Universal Medicap Ltd.)·Device Class Class D·India CDSCO·Brand: SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET
Registration details
UID
MFG/MD/2021/000346_aa06224a93603254ed27e23dc93903e5_fbfb3c75aa9abfd9ec2e56eb16cbc67a
Device class
Class D
Brand name
SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET
License holder
M/s. Universal ISO-MED (A Div. of Universal Medicap Ltd.)
Approving authority
Central Drug Standards Control Organization, Ahmedabad
Product information
Oxidized Regenerated Cellulose Haemostat is designed to arrest capillary bleeding and bleeding from parenchymatous organs and resection areas at surgical interventions. It is suitable for use in general surgery and digestive surgery, neurosurgery (SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET), plastic surgery, orthopaedic, gynaecology, urology, stomatology, traumatology, and many other branches of surgery. Oxidized Regenerated Cellulose Haemostat can be applied into cavities (SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET) as well as endoscopic interventions or dental praxis. Oxidized Regenerated Cellulose Haemostat is used adjunctively in various surgical procedures to assist when control of bleeding from capillary, venous and small arteriolar vessels, by pressure, ligature and other conventional procedures is either ineffective or impractical. The Oxidized Regenerated Cellulose Haemostat can be cut to size in endoscopic procedures.
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About this record

Oxidized Regenerated Cellulose Haemostat is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000346_aa06224a93603254ed27e23dc93903e5_fbfb3c75aa9abfd9ec2e56eb16cbc67a. This device is marketed under the brand name SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET. The license holder is M/s. Universal ISO-MED (A Div. of Universal Medicap Ltd.), and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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