Saudi Arabia SFDA registration ME0000002519SFDAA00251
Jaws "HiQ+". 5 x 430 mm, Johann
Product information
ENDOSCOPY INSTRUMENTS
Product use
Jaws insert for HiQ+ hand instruments.
Device classification
- Risk Class
- Class IIb
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000002519SFDAA00251
- Authorization ID
- GHTF-2015-0531
- Status
- Active
- Expire Date
- May 27, 2020
Manufacturer
- Manufacturer Name
- Olympus Winter & lbe GmbH
Model information
- Model ID(s)
- WA64120L
Product accessories
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About this record
Access comprehensive regulatory information for Jaws "HiQ+". 5 x 430 mm, Johann in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000002519SFDAA00251 and manufactured by Olympus Winter & lbe GmbH.
This page provides complete registration details including product category (Medical Device), 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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb