CDSCO UID MFG/IVD/2019/000061_ffa390385f17a2f8cf9e11de41839d63_cc95975df44e9f4cd86ec6fe562da98d
Stained Salmonella Antigen Set : For Widal Test
ARKRAY HEALTHCARE PVT. LTD.·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2019/000061_ffa390385f17a2f8cf9e11de41839d63_cc95975df44e9f4cd86ec6fe562da98d
- Device class
- Class B
- License holder
- ARKRAY HEALTHCARE PVT. LTD.
- Approving authority
- Gujarat
- Product information
- Diagnostic reagents for the in vitro detection and quantitative estimation of specific antibodies to Salmonella present in serum by rapid slide and conventional tube tests
Similar products (1)
Other products with the same name or brand
Stained Salmonella Antigen Set : For Widal Test
ARKRAY HEALTHCARE PVT. LTD.
Class B
Other products from ARKRAY HEALTHCARE PVT. LTD.
Products from the same license holder (10 products)
Cefuroxime Sensitivity Disc , 30 µg/ Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Stained Salmonella Antigen Set : For Widal Test
Class B
Piperacillin / tazobactum Sensitivity Disc , 100 + 10 µg/ Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Amoxycillin / clavulanic acid Sensitivity Disc , 20+10 µg/ Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Co-Trimoxazole Sensitivity Disc , 25 µg/Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Sodium: Trinder's, Potassium : Tetraphenyl Boron, End Point Assay
Brand: AutoSpan Liquid Gold Lipase
Class B
Tetracycline Sensitivity Disc , 30 μg / Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Stained Salmonella S. typhi ‘H’ Antigen : For Widal test
Class B
Cefixime Sensitivity Disc , 5 µg/ Disc
Brand: AutoSpan Liquid Gold Lipase
Class B
Selective Detergent, End Point Assay
Brand: AutoSpan Liquid Gold Lipase
Class B
About this record
Stained Salmonella Antigen Set : For Widal Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000061_ffa390385f17a2f8cf9e11de41839d63_cc95975df44e9f4cd86ec6fe562da98d. The license holder is ARKRAY HEALTHCARE PVT. LTD., and it is classified as Device Class Class B. The approving authority is Gujarat.
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.