Taiwan FDA registration e0b9b5dab154f8d0e82d07175607c6f8

"Leishi" dream silicone mask

TW: “磊仕＂助夢矽膠面罩

Taiwan·Risk Class 2·RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.·Registered Nov 11, 2022 – Nov 11, 2027Active

Registration details

Analysis ID: e0b9b5dab154f8d0e82d07175607c6f8
Customs Code: DHA09200139804

Company information

Manufacturer: RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.
Manufacturer Country: United States;;China
Authorized Representative: PHILIPS TAIWAN LIMITED

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5905 Non-continuous respirators
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Nov 11, 2022
Expiry Date: Nov 11, 2027

About this record

Access comprehensive regulatory information for "Leishi" dream silicone mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0b9b5dab154f8d0e82d07175607c6f8 and manufactured by RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SZ) CO., LTD.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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