Pure Global

WIDAL TUBE TEST - India CDSCO Medical Device Registration

WIDAL TUBE TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000072_e6dcc1427e7920a608ad61b33d844870_d168d23123d7195e3c5a28347556b200. The license holder is DELTA LAB, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
WIDAL TUBE TEST
UID: MFG/MD/2022/000072_e6dcc1427e7920a608ad61b33d844870_d168d23123d7195e3c5a28347556b200

License Holder

DELTA LAB

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The WIDAL TUBE Test is intended for In Vitro quantitative determination of antibodies ##PLACEHOLDER_0## in a blood sample against two antigens ##PLACEHOLDER_0## of bacteria, Salmonella enterica in human serum. Widal TUBE Test is used for professional in vitro diagnostic use only

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand