CDSCO UID MFG/IVD/2023/000049_934f9c3ed6c23ea567ce779f636298fa_9af775396ad9fc52efba40ba83c79f27
Rinse
Lord's Mark Industries Pvt. Ltd.·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2023/000049_934f9c3ed6c23ea567ce779f636298fa_9af775396ad9fc52efba40ba83c79f27
- Device class
- Class B
- License holder
- Lord's Mark Industries Pvt. Ltd.
- Approving authority
- Kokan Division
- Product information
- It is used for cleaning and rinsing of fluidic path of Blood cell counter
Similar products (9)
Other products with the same name or brand
Rinse
Precilab Reagents And Chemicals Pvt Ltd
Class B
Rinse
Brand: DSA
M/s Avantor Performance Materials India Private Limited
Class B
Rinse
Brand: UniLyse - 530/620
UNIWORTH LABORATORY
Class B
Rinse
Brand: 3 part Differential
Promea Therapeutics Private Limited
Class B
Rinse
Brand: 3 part Differential
Promea Therapeutics Private Limited
Class B
Rinse
Brand: BIOGENIX
Biogenix Inc. Pvt. Ltd.
Class B
Rinse
Brand: sVNT
ASPEN LABORATORIES PRIVATE LIMITED
Class B
Rinse
Brand: 3 Part Differential
Avantor Performance Materials India Limited
Class B
Rinse
Brand: IL6
KARWA ENTERPRISES PRIVATE LIMITED
Class B
Other products from Lord's Mark Industries Pvt. Ltd.
Products from the same license holder (10 products)
Total Bile Acid
Brand: LordsMed Homocysteine Reagent
Class B
Ammonia Reagent
Brand: LordsMed Homocysteine Reagent
Class B
Urea UV Test kit
Class B
Phosphorus Test Kit
Class B
Dengue IgG/ IgM Antibody Rapid Test
Brand: LordsMed Homocysteine Reagent
Class B
Triglycerides Test Kit
Class B
Glucose Test Kit
Class B
3 Part Hematology Analyzer
Brand: LordsMed Semi Auto biochemistry Analyzer
Class A
Bilirubin Test Kit
Brand: LordsMed Homocysteine Reagent
Class B
Potassium Test Kit
Class B
About this record
Rinse is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000049_934f9c3ed6c23ea567ce779f636298fa_9af775396ad9fc52efba40ba83c79f27. The license holder is Lord's Mark Industries 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.