Nasal file/rasp - UK MHRA Medical Device Registration

Nasal file/rasp is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 208351. The device is manufactured by SPIGGLE & THEIS Medizintechnik GmbH from Germany, 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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Nasal file/rasp

MHRA Device ID: 208351

Device Type

General Medical Device

Type

Class I

Status

DREGIY

Date Registered

Jan 14, 2025

Manufacturer Information

Name

SPIGGLE & THEIS Medizintechnik GmbH

Address

Burghof 14

Overath, Germany

DJ Fang

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Other Products from SPIGGLE & THEIS Medizintechnik GmbH (10)

Nasal file/rasp - UK MHRA Medical Device Registration

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

Bone distraction forceps

Arthrodesis nail

Hypnotherapy virtual reality software

Internal orthopaedic fixation system, cerclage wire/cable, sterile

Multidisciplinary medical image management software

Patient transfer assistive bed/mobile chair

Nasal irrigation saline solution

Surgical microscope filter

Decontamination floor mat, single-use

Compression/pressure sock/stocking, single-use

Intranasal splint, non-biodegradable

Instrument tray, reusable

Pressure bandage, non-latex, single-use

Surgical snare wire

Suturing needle holder, reusable

Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Tonsil scissors

Tissue injection cannula

Vascular scissors

Surgical irrigation tubing set, single-use