United Kingdom MHRA device registration 207951

Digital storage media

United Kingdom·General Medical Device·LumiThera, Inc.·Registered Jan 3, 2025DREGIY

Registration details

Device ID: 207951
Status: DREGIY
Date Registered: Jan 3, 2025

Device classification

Device Type: General Medical Device
Type: Class I

Manufacturer

Name: LumiThera, Inc.
Address: 19578 10th Avenue NE, Suite 200
Poulsbo, Washington, United States

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About this record

Digital storage media is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207951. The device is manufactured by LumiThera, Inc. from United States, classified as General Medical Device.

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