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Forceps, throughcutting - SFDA Registration ME0000003595SFDAA00050

Access comprehensive regulatory information for Forceps, throughcutting in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000003595SFDAA00050 and manufactured by KARL STORZ SE & Co. KG.

This page provides complete registration details including product category (Medical Device), manufacturer information, 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 I
ME0000003595SFDAA00050
Forceps, throughcutting
SFDA Registration: ME0000003595SFDAA00050
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Product Information

Throughcutting Forceps or Punch Instrument

Product Use

Used to separate, cut and remove tissue, cartilage or bone for diagnostic measures and surgical interventions.

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003595SFDAA00050
Authorization ID
GHTF-2017-1375
Status
Active
Expire Date
November 03, 2020
Manufacturer
Manufacturer Name
KARL STORZ SE & Co. KG
Product Accessories

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