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"Leishi" humid heater - Taiwan Registration d5afa91f6448c3b7bd6f1aa95e3406a1

Access comprehensive regulatory information for "Leishi" humid heater in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d5afa91f6448c3b7bd6f1aa95e3406a1 and manufactured by RESPIRONICS INC.;; Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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d5afa91f6448c3b7bd6f1aa95e3406a1
Registration Details
Taiwan FDA Registration: d5afa91f6448c3b7bd6f1aa95e3406a1
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Device Details

"Leishi" humid heater
TW: "็ฃŠไป•"ๆฝฎๆฟ•ๅŠ ็†ฑๅ™จ
Risk Class 2

Registration Details

d5afa91f6448c3b7bd6f1aa95e3406a1

DHA05602853301

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5450 Vapor moisture apparatus for respirators

import

Dates and Status

May 12, 2016

May 12, 2026