Basic endotracheal tube, single-use - UK MHRA Medical Device Registration
Basic endotracheal tube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210800. The device is manufactured by Well Lead Medical 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 IIa
Status
Date Registered
Feb 14, 2025
Address
C-4 Jinhu Industrial Estate, Hualong, Panyu
Guangzhou, China
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Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Intermittent urethral drainage catheter, non-antimicrobial, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Single-administration urethral drainage/irrigation catheter
Type: General Medical Device
Registered: Feb 14, 2025
Reinforced endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025
Basic endotracheal tube, single-use
Type: General Medical Device
Registered: Feb 14, 2025

