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Oxidized Regenerated Cellulose Haemostat - India CDSCO Medical Device Registration

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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CDSCO Registered
Class Class D
Oxidized Regenerated Cellulose Haemostat
UID: MFG/MD/2021/000346_aa06224a93603254ed27e23dc93903e5_fbfb3c75aa9abfd9ec2e56eb16cbc67a

Brand Name

SURGISPON, GELBOND, HEMALIMIT, NEXCARE, PREMISUT, SURGIVET

Device Class

Class D

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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