Pure Global

Jaws "HiQ+", 5 x 250mm, grasping forceps, claw type - SFDA Registration ME0000002519SFDAA00136

Access comprehensive regulatory information for Jaws "HiQ+", 5 x 250mm, grasping forceps, claw type in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000002519SFDAA00136 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.

Free Database
Powered by Pure Global AI
SFDA Official Data
Class IIa
ME0000002519SFDAA00136
Jaws "HiQ+", 5 x 250mm, grasping forceps, claw type
SFDA Registration: ME0000002519SFDAA00136
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Claw type Jaws Insert

Product Use

The handinstruments are intended to be used in laparoscopic and endoscopic diagnosis and treatment in the abdomen and thorax.

Device Classification
Risk Class
Class IIa
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000002519SFDAA00136
Authorization ID
GHTF-2018-1062
Status
Active
Expire Date
August 25, 2023
Manufacturer
Manufacturer Name
Olympus Winter & lbe GmbH
Model Information
Model ID(s)
WA64020S
Product Accessories

[]