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Monopolar Forceps - SFDA Registration ME0000005736SFDAA00150

Access comprehensive regulatory information for Monopolar Forceps 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 ME0000005736SFDAA00150 and manufactured by Conmed Corporation.

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.

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Class IIb
ME0000005736SFDAA00150
Monopolar Forceps
SFDA Registration: ME0000005736SFDAA00150
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Product Information

Electrosurgical forceps designed to be used for surgical procedures

Product Use

These reusable bipolar electrosurgical forceps are intended to grasp and coagulate (control bleeding) by use of high-frequency electrical current, in neurosurgical, ophthalmic, plastic, and reconstructive surgical procedures. Maximum voltage is not to exceed 300 V peak.Reusable forceps designed to conduct electrosurgical current to the operative site for desired surgical effect. These forceps are supplied non-sterile; process through cleaning and sterilization prior to first use and for up to a total of 20 uses.

Device Classification
Risk Class
Class IIb
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000005736SFDAA00150
Authorization ID
GHTF-2015-1089
Status
Active
Expire Date
June 18, 2018
Manufacturer
Manufacturer Name
Conmed Corporation
Model Information
Model ID(s)
60-0810-001 60-0812-001 60-0817-001 60-0821-001 60-0819-001
Product Accessories

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