United Kingdom MHRA device registration 209452

Bone file/rasp, reciprocating, single-use

United Kingdom flagUnited Kingdom·General Medical Device·Extremity Medical LLC·Registered Jan 24, 2025DREGIY
Registration details
Device ID
209452
Status
DREGIY
Date Registered
Jan 24, 2025
Device classification
Device Type
General Medical Device
Type
Class IIa
Manufacturer
Address
Extremity Medical LLC, 3000 Interpace Parkway, Building A, 2nd Floor
Parsippany, NJ , United States
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About this record

Bone file/rasp, reciprocating, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209452. The device is manufactured by Extremity Medical LLC 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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