Rigid endoscopic tissue manipulation forceps, single-use - UK MHRA Medical Device Registration

Rigid endoscopic tissue manipulation forceps, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 213588. The device is manufactured by Teleflex Medical from United States, 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.

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General Medical Device

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Rigid endoscopic tissue manipulation forceps, single-use

MHRA Device ID: 213588

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Mar 18, 2025

Manufacturer Information

Name

Teleflex Medical

Address

3015 Carrington Mill Boulevard

Morrisville, North Carolina, United States

DJ Fang

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Rigid endoscopic tissue manipulation forceps, single-use - UK MHRA Medical Device Registration

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