Taiwan FDA registration 1dbfa78b3807d4a5ce53c035cbdde839

"Guomu" compressor type atomizer

TW: "國睦" 壓縮機型霧化器
Taiwan flagTaiwan·Risk Class 2·Guomu Industry Co., Ltd. General Factory·Registered Nov 23, 2004 – Nov 23, 2019Cancelled
Registration details
Analysis ID
1dbfa78b3807d4a5ce53c035cbdde839
Customs Code
DHY00500120202
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
D Anesthesiology
Import Information
Domestic
Dates and status
Registration Date
Nov 23, 2004
Expiry Date
Nov 23, 2019
Cancellation Date
Oct 15, 2019
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Guomu" compressor type atomizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1dbfa78b3807d4a5ce53c035cbdde839 and manufactured by Guomu Industry Co., Ltd. General Factory. The authorized representative in Taiwan is Guomu Industry Co., Ltd. General Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MERITS HEALTH PRODUCTS 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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