Gastrostomy procedure kit - UK MHRA Medical Device Registration
Gastrostomy procedure kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208935. The device is manufactured by Applied Medical Technology, Inc. from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Type
Class IIa
Status
Date Registered
Jan 17, 2025
Address
8006 Katherine Blvd.
Brecksville, OH, United States
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