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Versatus-S Plus - SFDA Registration ME0000000975SFDAA00098

Access comprehensive regulatory information for Versatus-S Plus 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 ME0000000975SFDAA00098 and manufactured by Terumo Europe N.V..

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 IIa
ME0000000975SFDAA00098
Versatus-S Plus
SFDA Registration: ME0000000975SFDAA00098
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Product Information

Intravenous Catheter

Product Use

The I.V. catheters are sterile, single use over-the-needle peripheral intravascular with a straight or winged hub and with or without injection site, made of plastic materials and stainless steel, intended for accessing the peripheral vascular system. The short peripheral catheter is intended to remain in place for 72 to 96 hours according to good clinical practice, the continuous use however would rarely exceed 30 days in common practice. The optional Surshield protector is intended to cover the exposed needle immediately after use to prevent needle stick injury.

Device Classification
Risk Class
Class IIa
Product Category
MD
Product Type
MD
Registration Information
Registration ID
ME0000000975SFDAA00098
Authorization ID
GHTF-2019-0456
Status
Active
Expire Date
November 18, 2023
Manufacturer
Manufacturer Name
Terumo Europe N.V.
Model Information
Model ID(s)
SR+DU2619SX SR+DU2419SX SR+DU2225SX SR+DU2032SX SR+DU1832SX SR+DU1845SX SR+DU1745SX SR+DU1645SX SR+DU1445SX
Product Accessories

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