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Absorbable Haemostatic Gelatin Sponge - India CDSCO Medical Device Registration

Absorbable Haemostatic Gelatin Sponge is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000148_4733d03f0b6196bdb0c006240649f0c5_fb4b830ce5422f64186ebc586fc93afa. This device is marketed under the brand name ANGISPONGE, STERISPON, TRUSPONGE, PREVASPONGE, STELLI GEL, ANGIPLAST, ANGIFOAM, ANGIPAD. The license holder is ELECTRO MAGNETIC INDUSTRIES, 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
Absorbable Haemostatic Gelatin Sponge
UID: MFG/MD/2023/000148_4733d03f0b6196bdb0c006240649f0c5_fb4b830ce5422f64186ebc586fc93afa

Brand Name

ANGISPONGE, STERISPON, TRUSPONGE, PREVASPONGE, STELLI GEL, ANGIPLAST, ANGIFOAM, ANGIPAD

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

ANGISPONGE can be effectively used in various surgeries for haemostasis, when control of capillary, venous and arteriolar bleeding by pressure, ligature and other conventional procedures is ineffective or impractical. ANGISPONGE may be used dry or saturated with physiological salt solution. Cut to the desired size, a piece of ANGISPONGE, either dry or saturated with sterile, isotonic sodium chloride solution (ANGISPONGE, STERISPON, TRUSPONGE, PREVASPONGE, STELLI GEL, ANGIPLAST, ANGIFOAM, ANGIPAD), can be applied with light pressure directly to the bleeding site. When applied dry, a single piece of ANGISPONGE should be manually applied to the bleeding site, and held in place with moderate pressure until haemostatic results

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