Luteinizing Hormone Rapid Test
- UID
- MFG/IVD/2023/000113_c55378125c7d56372c606041ffdf9efb_e78652c07bc282cd6170f57c89aaa8b0
- Device class
- Class B
- Brand name
- Chimera
- License holder
- CHIMERA BIOTECH PRIVATE LIMITED
- Approving authority
- South Delhi Division
- Product information
- The Chimera® LH Test is a rapid immuno-chromatographic assay for the qualitative detection of luteinizing hormone (Chimera) in urine. This test is for in vitro screening used in obtaining a visual qualitative result for LH in urine to predict the time of ovulation.
Luteinizing Hormone Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_c55378125c7d56372c606041ffdf9efb_e78652c07bc282cd6170f57c89aaa8b0. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi Division.
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