Polyolefin/fluoropolymer suture, multifilament - UK MHRA Medical Device Registration

Polyolefin/fluoropolymer suture, multifilament is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208876. The device is manufactured by Riverpoint Medical, LLC from United States, classified as General Medical Device.

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Polyolefin/fluoropolymer suture, multifilament

MHRA Device ID: 208876

Device Type

General Medical Device

Type

Class IIb

Status

DREGIY

Date Registered

Jan 17, 2025

Manufacturer Information

Name

Riverpoint Medical, LLC

Address

825 NE 25th Ave

Portland, Oregon, United States

DJ Fang

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Polyolefin/fluoropolymer suture, multifilament - UK MHRA Medical Device Registration

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