Periodontal file/rasp, manual - UK MHRA Medical Device Registration

Periodontal file/rasp, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 158077. The device is manufactured by Hu-Friedy Mfg. Co.,LLC from United States, classified as General Medical Device. The authorized representative in the UK is STERIS Solutions Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, 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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Periodontal file/rasp, manual

MHRA Device ID: 158077•Ref: 158077

Device Type

General Medical Device

Devices

Periodontal file/rasp, manual

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 25, 2024

Manufacturer Information

Name

Hu-Friedy Mfg. Co.,LLC

Address

3232 N Rockwell St.

Chicago, IL, United States

Created Date

Oct 13, 2022

Authorized Representative

Name

STERIS Solutions Limited

Relationship Type

UK Responsible Person

Address

Chancery House, Rayns Way Watermead Business Park Syston

Leicester, Leicestershire, England, United Kingdom

Postcode: LE7 1PF

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Periodontal file/rasp, manual - UK MHRA Medical Device Registration

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Date Registered

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