United Kingdom MHRA device registration 211542

Endoscope sheath, reusable

United Kingdom·General Medical Device·Stryker Endoscopy, a division of Stryker Corporation·Registered Feb 21, 2025DREGIY

Registration details

Device ID: 211542
Status: DREGIY
Date Registered: Feb 21, 2025

Device classification

Device Type: General Medical Device
Type: Class I

Manufacturer

Name: Stryker Endoscopy, a division of Stryker Corporation
Address: 5900 Optical Ct
San Jose, United States

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About this record

Endoscope sheath, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 211542. The device is manufactured by Stryker Endoscopy, a division of Stryker Corporation from United States, classified as General Medical Device.

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