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Aspisafe - India CDSCO Medical Device Registration

Aspisafe is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000148_cc429fadd42737d0c0904e1308ed60dd_83213a65e5eb0392ef627a94c0975621. This device is marketed under the brand name Dermafilm & Dermincise. The license holder is VYGON INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Aspisafe
UID: IMP/MD/2019/000148_cc429fadd42737d0c0904e1308ed60dd_83213a65e5eb0392ef627a94c0975621

Brand Name

Dermafilm & Dermincise

Device Class

Class B

Approving Authority

CDSCO

Product Information

Catheter for protected distal bronchial sampling for diagnosis of ventilator-associated pneumonia in intensive care of patients mechanically ventilated

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