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CDSCO UID IMP/MD/2020/000124_0f5035ac92125382fe2dd659a6db8e07_43165fbc402c4e502bc4b1a9384150c7

Hemostat

Johnson & Johnson Private Limited·Device Class Class D·India CDSCO·Brand: SPONGOSTAN Absorbable Haemostatic Gelatin Sponge
Registration details
UID
IMP/MD/2020/000124_0f5035ac92125382fe2dd659a6db8e07_43165fbc402c4e502bc4b1a9384150c7
Device class
Class D
Brand name
SPONGOSTAN Absorbable Haemostatic Gelatin Sponge
License holder
Johnson & Johnson Private Limited
Approving authority
CDSCO
Product information
SPONGOSTAN Powder, saturated with sterile sodium chloride solution, is indicated for surgical procedures (SPONGOSTAN Absorbable Haemostatic Gelatin Sponge) for haemostasis, when control of capillary bleeding, oozing bleeding, venous and arteriolar bleeding by pressure, ligature and other conventional procedures is ineffective or impractical. Although not necessary, SPONGOSTAN Powder can be used with thrombin to achieve haemostasis
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About this record

Hemostat is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000124_0f5035ac92125382fe2dd659a6db8e07_43165fbc402c4e502bc4b1a9384150c7. This device is marketed under the brand name SPONGOSTAN Absorbable Haemostatic Gelatin Sponge. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

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