Taiwan FDA registration dd8f16295922e8c6567aa5edaeec9f1e

"Leishi" comfort mask

TW: “磊仕”舒適面罩
Taiwan flagTaiwan·Risk Class 2·Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.·Registered Aug 01, 2012 – Aug 01, 2022Cancelled
Registration details
Analysis ID
dd8f16295922e8c6567aa5edaeec9f1e
Customs Code
DHA04200045403
Company information
Manufacturer Country
United States;;China
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
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
Aug 01, 2012
Expiry Date
Aug 01, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Leishi" comfort mask in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dd8f16295922e8c6567aa5edaeec9f1e and manufactured by Respironics Inc.;; Respironics Medical Products(Shenzhen)Co., Ltd.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RESPIRONICS INC.;; RESPIRONICS MEDICAL PRODUCTS (SHENZHEN) CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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