Needle guide, single-use - UK MHRA Medical Device Registration

Needle guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207668. The device is manufactured by TSK Laboratory, Japan from Japan, classified as General Medical Device.

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MHRA Registered

General Medical Device

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Needle guide, single-use

MHRA Device ID: 207668

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Dec 24, 2024

Manufacturer Information

Name

TSK Laboratory, Japan

Address

1510-1 Soja-machi

Tochigi-Shi, Tochigi-Ken, Japan

DJ Fang

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Needle guide, single-use - UK MHRA Medical Device Registration

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Name

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