United Kingdom MHRA device registration 213288

Aneroid manual sphygmomanometer

United Kingdom flagUnited Kingdom·General Medical Device·Koven Technology, Inc. ·Registered Mar 13, 2025DREGIY
Registration details
Device ID
213288
Status
DREGIY
Date Registered
Mar 13, 2025
Device classification
Device Type
General Medical Device
Type
Class IIa
Manufacturer
Address
477 N Lindbergh Blvd, Suite 220
St Louis, Missouri, United States
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About this record

Aneroid manual sphygmomanometer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 213288. The device is manufactured by Koven 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.

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