United Kingdom MHRA device registration 163408
Pelvic organ prolapse surgical mesh, synthetic polymer
United Kingdom·General Medical Device·Coloplast AS·Registered Apr 23, 2021Registration details
- Device ID
- 163408
- MHRA Reference Number
- 163408
- Date Registered
- Apr 23, 2021
- Last Updated
- Mar 11, 2023
Device classification
- Device Type
- General Medical Device
- Devices
- Pelvic organ prolapse surgical mesh, synthetic polymer
- Type
- Class III
Manufacturer
- Name
- Coloplast AS
- Address
- Holtedam 1 Humlebaek, Denmark
- Created Date
- Apr 23, 2021
Authorized Representative
- Name
- Coloplast Ltd
- Relationship Type
- UK Responsible Person
- Address
- Nene Hall Peterborough Business Park Peterborough, Cambridgeshire, England, United KingdomPostcode: PE2 6FX
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About this record
Pelvic organ prolapse surgical mesh, synthetic polymer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163408. The device is manufactured by Coloplast AS from Denmark, classified as General Medical Device. The authorized representative in the UK is Coloplast Ltd.
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