Taiwan FDA registration 3d175bdb62e97a610f8e5b1ed3aec66e

"Veali" endotracheal probe (sterilized/unsterilized)

TW: "維立" 氣管內管探針 (滅菌/未滅菌)

Taiwan·Risk Class 1·Well Lead Medical Co., Ltd.·Registered Feb 27, 2019 – Feb 27, 2029Active

Registration details

Analysis ID: 3d175bdb62e97a610f8e5b1ed3aec66e
Customs Code: DHA09600370108

Company information

Manufacturer: Well Lead Medical Co., Ltd.
Manufacturer Country: China
Authorized Representative: TAIWAN MEDICAL SERVICES CORPORATION

Product details

Intended Use: Limited to the first level identification range of the "endotracheal tube probe (D.5790)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5790 氣管內管探針
Import Information: Chinese goods;; QMS/QSD;; input

Dates and status

Registration Date: Feb 27, 2019
Expiry Date: Feb 27, 2029

About this record

Access comprehensive regulatory information for "Veali" endotracheal probe (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3d175bdb62e97a610f8e5b1ed3aec66e and manufactured by Well Lead Medical Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.

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