Saudi Arabia SFDA registration ME0000002780SFDAA00246
BOND Lambda Probe, 5.5 mL
Product information
Lambda Probe
Product use
Lambda Probe is intended for use in the qualitative identification of Lambda light chain messenger RNA (mRNA) in formalin-fixed,
paraffin-embedded tissue by in situ hybridization (ISH) using the automated BOND system.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000002780SFDAA00246
- Authorization ID
- MDMA-1-2019-4548
- Status
- Active
- Expire Date
- May 27, 2025
Manufacturer
- Manufacturer Name
- Leica Biosystems Newcastle Ltd
Model information
- Model ID(s)
- PB0669
Product accessories
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About this record
Access comprehensive regulatory information for BOND Lambda Probe, 5.5 mL in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000002780SFDAA00246 and manufactured by Leica Biosystems Newcastle Ltd.
This page provides complete registration details including product category (Chemicals), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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