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"Centrum" Flexible Laryngoscope (Non-Sterile) - Taiwan Registration 6aae0da7d255a87d290062d1e42400cc

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..

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6aae0da7d255a87d290062d1e42400cc
Registration Details
Taiwan FDA Registration: 6aae0da7d255a87d290062d1e42400cc
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Device Details

"Centrum" Flexible Laryngoscope (Non-Sterile)
TW: "ไป™ๆทณ" ๅฏๅฝŽๆ›ฒๅผๅ–‰้ ญ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6aae0da7d255a87d290062d1e42400cc

Ministry of Health Medical Device Import No. 018803

DHA09401880305

Company Information

Product Details

Limited to the first level of identification range of "Flexible Laryngoscope (D.5530)" under the Measures for the Administration of Medical Devices.

D Devices for anesthesiology

D5530 Flexible laryngoscope

Imported from abroad

Dates and Status

Feb 08, 2018

Feb 08, 2023