Saudi Arabia SFDA registration ME0000002519SFDAA00140
Shaft "HiQ+", bipolar, 5 x 330mm, insulated
Saudi Arabia·MD·Olympus Winter & lbe GmbH·Class IIActiveProduct information
BIPOLAR HAND INSTRUMENT
Product use
For laparoscopic and endoscopic diagnosis and treatment in the
abdomen and thorax.
• Do not use for any other purposes.
Device classification
- Risk Class
- Class II
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000002519SFDAA00140
- Authorization ID
- GHTF-2020-0901
- Status
- Active
- Expire Date
- April 15, 2023
Manufacturer
- Manufacturer Name
- Olympus Winter & lbe GmbH
Model information
- Model ID(s)
- WA60800C
Product accessories
[]
About this record
Access comprehensive regulatory information for Shaft "HiQ+", bipolar, 5 x 330mm, insulated in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000002519SFDAA00140 and manufactured by Olympus Winter & lbe GmbH.
This page provides complete registration details including product category (MD), 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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