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.

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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

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Patient transfer assistive bed/mobile chair

Arthroplasty force sensor

Cervicothoracolumbosacral spine orthosis, rigid

Hypnotherapy virtual reality software

Multidisciplinary medical image management software

Radiology PACS software

Scanning-laser ophthalmic imaging system

Dental implant abutment trial

Arthrodesis nail

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