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UNIMED Procedure Pack ENT Pack Adult ENT Pack - SFDA Registration ME0000002294SFDAA00377

Access comprehensive regulatory information for UNIMED Procedure Pack ENT Pack Adult ENT Pack in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000002294SFDAA00377 and manufactured by United Medical Industries Limited Co. L.L.C.

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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SFDA Official Data
1
ME0000002294SFDAA00377
UNIMED Procedure Pack ENT Pack Adult ENT Pack
SFDA Registration: ME0000002294SFDAA00377
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Product Information

Sterile single use pack having gowns drapes covers bags sheets needle counters and towels

Device Classification
Risk Class
1
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000002294SFDAA00377
Authorization ID
MDMA-2-2025-0588
Status
Active
Expire Date
February 21, 2028
Manufacturer
Model Information
Model ID(s)
UMIPP0014,UMIPP0014 V1,UMIPP0014 V2,UMIPP0014 V3,UMIPP0014 V4,UMIPP0014 V5,UMIPP0014 V6,UMIPP0014 V7
Product Accessories

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