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Endometrial Biopsy Curette - India CDSCO Medical Device Registration

Endometrial Biopsy Curette is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000853_aff5cfccad1936d41b0a958793aec066_f5f8b18532d8b342e161a1ed28e3b01e. This device is marketed under the brand name ESA, Andalan Histerometro, Flexi T. The license holder is M/S A. V. Processors Pvt. Ltd.,, 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
Endometrial Biopsy Curette
UID: MFG/MD/2023/000853_aff5cfccad1936d41b0a958793aec066_f5f8b18532d8b342e161a1ed28e3b01e

Brand Name

ESA, Andalan Histerometro, Flexi T

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The Accurette Endometrial Biopsy Curette is intended for the removal of endometrial tissue for biopsy sample.

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