Taiwan FDA registration 7f35b0e8594a1dd8cace545f33fc56db

"Laerdal" Tracheal Tube Fixation Device (Non-Sterile)

TW: "雷德"氣管管路固定裝置(未滅菌)

Taiwan·Risk Class 1·MD·LAERDAL MEDICAL CORPORATION·Registered Oct 20, 2020 – Oct 20, 2025Expired

Registration details

Analysis ID: 7f35b0e8594a1dd8cace545f33fc56db
License Form: Ministry of Health Medical Device Import No. 022046
Customs Code: DHA09402204606

Company information

Manufacturer: LAERDAL MEDICAL CORPORATION
Manufacturer Country: United States
Authorized Representative: FU SHING MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5770 Tracheal Line Fixture
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 20, 2020
Expiry Date: Oct 20, 2025

About this record

Access comprehensive regulatory information for "Laerdal" Tracheal Tube Fixation Device (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 7f35b0e8594a1dd8cace545f33fc56db and manufactured by LAERDAL MEDICAL CORPORATION. The authorized representative in Taiwan is FU SHING MEDICAL CO., LTD..

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