Saudi Arabia SFDA registration ME0000002519SFDAA00257
Jaws "HiQ+", 5 x 330 mm, dissection forceps, straight
Saudi Arabia·Medical Device·Olympus Winter & lbe GmbH·Class IIbActiveProduct information
Dissection Forceps
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
- ME0000002519SFDAA00257
- Authorization ID
- GHTF-2015-0532
- Status
- Active
- Expire Date
- August 25, 2020
Manufacturer
- Manufacturer Name
- Olympus Winter & lbe GmbH
Model information
- Model ID(s)
- A64310A
Product accessories
[]
About this record
Access comprehensive regulatory information for Jaws "HiQ+", 5 x 330 mm, dissection forceps, straight 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 ME0000002519SFDAA00257 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