CDSCO UID IMP/MD/2023/000170_37e350627eb920f9c3654fad2e80a6e0_0d54ae9fb7dba1fe784814b92dbc46ab

Surgical Wound Dressing

Varvie Meditech Private Limited,·Device Class Class A·India CDSCO·Brand: Curapor® Transparent
Registration details
UID
IMP/MD/2023/000170_37e350627eb920f9c3654fad2e80a6e0_0d54ae9fb7dba1fe784814b92dbc46ab
Device class
Class A
Brand name
Curapor® Transparent
Approving authority
CDSCO
Product information
Curapor® surgical dressing is intended for postoperative, acute and superficial wound care, as well as cuts and lacerations
Similar products (5)
Other products with the same name or brand
Cannula Retention Dressing
Brand: Curapor® Transparent
Varvie Meditech Private Limited,
Class A
Cannula Retention Dressing
Brand: Curapor® Transparent
Varvie Meditech Private Limited,
Class A
Cannula Retention Dressing
Brand: Curapor® Transparent
Varvie Meditech Private Limited,
Class A
Transparent Surgical Wound Dressing
Brand: Curapor® Transparent
Varvie Meditech Private Limited,
Class A
Surgical Wound Dressing
Brand: Curapor®
Triage Meditech Pvt. Ltd
Class B
Other products from Varvie Meditech Private Limited,
Products from the same license holder (10 products)
Surgical drapes and covers
Brand: Raucodrape® Pro
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Surgical drapes and covers
Brand: Raucodrape® Pro
Class B
Surgical gowns
Brand: Raucodrape® Pro
Class B
Cannula Retention Dressing
Brand: Curapor® Transparent
Class A
Cannula Retention Dressing
Brand: Curapor® Transparent
Class A
Cannula Retention Dressing
Brand: Curapor® Transparent
Class A
Transparent Surgical Wound Dressing
Brand: Curapor® Transparent
Class A
Biopsy Needle
Brand: Epidural Kit
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Central Venous Catheters Kits
Brand: Central Venous Catheters Kits
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Dialysis Catheters Short Term
Brand: Epidural Kit
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About this record

Surgical Wound Dressing is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000170_37e350627eb920f9c3654fad2e80a6e0_0d54ae9fb7dba1fe784814b92dbc46ab. This device is marketed under the brand name Curapor® Transparent. The license holder is Varvie Meditech Private Limited,, and it is classified as Device Class Class A. The approving authority is CDSCO.

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