Taiwan FDA registration 6aae0da7d255a87d290062d1e42400cc

"Centrum" Flexible Laryngoscope (Non-Sterile)

TW: "仙淳" 可彎曲式喉頭鏡 (未滅菌)

Taiwan·Risk Class 1·MD·CENTRUM DIS TIC. & ELEKTRONIK SAN. LTD. STI.·Registered Feb 08, 2018 – Feb 08, 2023Expired

Registration details

Analysis ID: 6aae0da7d255a87d290062d1e42400cc
License Form: Ministry of Health Medical Device Import No. 018803
Customs Code: DHA09401880305

Company information

Manufacturer: CENTRUM DIS TIC. & ELEKTRONIK SAN. LTD. STI.
Manufacturer Country: Turkey
Authorized Representative: TRANSMEDIC CO., LTD.

Product details

Intended Use: Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5530 Flexible laryngoscope
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 08, 2018
Expiry Date: Feb 08, 2023

About this record

Access comprehensive regulatory information for "Centrum" Flexible Laryngoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6aae0da7d255a87d290062d1e42400cc and manufactured by CENTRUM DIS TIC. & ELEKTRONIK SAN. LTD. STI.. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.