Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

Dental/maxillofacial surgical procedure kit, non-medicated, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 158105. 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.

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Dental/maxillofacial surgical procedure kit, non-medicated, reusable

MHRA Device ID: 158105•Ref: 158105

Device Type

General Medical Device

Devices

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

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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Other Products from Hu-Friedy Mfg. Co.,LLC (10)

Other Products from Same Authorized Representative (10)

Dental/maxillofacial surgical procedure kit, non-medicated, reusable - UK MHRA Medical Device Registration

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