Bone file/rasp, manual, reusable - UK MHRA Medical Device Registration
Bone file/rasp, manual, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181439. The device is manufactured by Normmed Medikal Sanayi ve Ticaret A.S. from Turkey, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices LTD.
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.
Device Type
General Medical Device
Devices
Bone file/rasp, manual, reusable
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Aug 30, 2024
Address
Ivedik Osb Mah. Havalandirmacilar Cad. No.193 Yenimahalle
Ankara, Turkey
Created Date
Nov 8, 2023
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
General-body orifice lubricant, non-sterile
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Manufacturer: Turkuaz Saฤlฤฑk Hizmetleri Medikal Temizlik Kimyasal รrรผnler Sanayi ve Ticaret A.ล.
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Type: General Medical Device
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Type: General Medical Device
Manufacturer: Moses Enterprises
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Type: General Medical Device
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Type: General Medical Device
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Type: General Medical Device
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Type: General Medical Device
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Manufacturer: Subtle Medical, Inc.
Abdominal/ENT/orthopaedic surgical probe, reusable
Type: General Medical Device
Manufacturer: Moses Enterprises

