United Kingdom MHRA device registration 208619

Suture knot pusher, single-use

United Kingdom·General Medical Device·Smith & Nephew, Inc., Endoscopy Division·Registered Jan 14, 2025DREGIY

Registration details

Device ID: 208619
Status: DREGIY
Date Registered: Jan 14, 2025

Device classification

Device Type: General Medical Device
Type: Class IIa

Manufacturer

Name: Smith & Nephew, Inc., Endoscopy Division
Address: 150 Minuteman Road
Andover, Massachusetts, United States

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About this record

Suture knot pusher, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208619. The device is manufactured by Smith & Nephew, Inc., Endoscopy Division from United States, classified as General Medical Device.

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