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CDSCO UID IMP/MD/2019/000547_1858772d9e163a944c336528df349b1e_a39065285df9b138edf9648ae02df1ba

For wound Debridement

Genetix Biotech Asia Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: Debrisoft® Lolly
Registration details
UID
IMP/MD/2019/000547_1858772d9e163a944c336528df349b1e_a39065285df9b138edf9648ae02df1ba
Device class
Class C
Brand name
Debrisoft® Lolly
License holder
Genetix Biotech Asia Pvt. Ltd.
Approving authority
CDSCO
Product information
Debrisoft® Lolly is intended for the debridement of deep – including surgically invasive – to superficial wounds for wound bed preparation e.g., diabetic ulcers, arterial and venous ulcers, pressure ulcers, postoperative wounds healing by secondary intention and trauma as well as burns / scalds. Debrisoft® Lolly can also be used to absorb exudate, debris and keratodermas during debridement.
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About this record

For wound Debridement is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000547_1858772d9e163a944c336528df349b1e_a39065285df9b138edf9648ae02df1ba. This device is marketed under the brand name Debrisoft® Lolly. The license holder is Genetix Biotech Asia Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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