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BIOHAZARD PACK - India CDSCO Medical Device Registration

BIOHAZARD PACK is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000697_ea10bc3a97a9a82269bce327daa18009_f16f4a5b4f7c18d1c9277d7a02f0c326. This device is marketed under the brand name REGAL. The license holder is REGAL HEALTHCARE, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
BIOHAZARD PACK
UID: MFG/MD/2023/000697_ea10bc3a97a9a82269bce327daa18009_f16f4a5b4f7c18d1c9277d7a02f0c326

Brand Name

REGAL

License Holder

REGAL HEALTHCARE

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Biohazard Pack and drape accessories is a device made of natural orsynthetic materials intended to be used as a protective patient covering to isolate a site of surgical incision from microbial and other contamination

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