Polyurethane examination/treatment glove, non-powdered - UK MHRA Medical Device Registration
Polyurethane examination/treatment glove, non-powdered is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207969. The device is manufactured by Zibo Blue Sail Health Technology Co., Ltd. from China, 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.
Device Type
General Medical Device
Type
Class I
Status
Date Registered
Jan 4, 2025
Address
No.1888 Honghua Road,High Technical Area,
Zibo, Shandong, China
External orthopaedic fixation system, single-use
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation system, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Cannulated surgical drill bit, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Bone-nailing spacer
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Cannulated surgical drill bit, single-use
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
External orthopaedic fixation system, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Bone nail guidewire, reusable
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Manual blood lancing device, single-use
Type: General Medical Device
Manufacturer: Tasso, Inc.
Bone nail guidewire, single-use
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Flexible bone nail
Type: General Medical Device
Manufacturer: Orthofix S.r.l.
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Type: General Medical Device
Registered: Nov 26, 2024
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Type: General Medical Device
Registered: Nov 26, 2024
Surgical/medical face mask, antimicrobial, single-use
Type: General Medical Device
Registered: Nov 26, 2024

