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Shaft "HiQ+", bipolar, 5 x 330mm, insulated - SFDA Registration ME0000002519SFDAA00140

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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Class II
ME0000002519SFDAA00140
Shaft "HiQ+", bipolar, 5 x 330mm, insulated
SFDA Registration: ME0000002519SFDAA00140
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Product Information

BIPOLAR HAND INSTRUMENT

Product Use

For laparoscopic and endoscopic diagnosis and treatment in the abdomen and thorax. โ€ข 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

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