Mah Respirator
Taiwan·PENLON LTD.·Registered Jan 21, 1987 – Jan 21, 1992Cancelled- Analysis ID
- fdd1bc096bac4b093fadce0922fd28dc
- Customs Code
- DHA00600453101
- Manufacturer
- PENLON LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Sankyo Trading Co., Ltd
- Product Type (Level 1)
- 0101 Anesthesia apparatus
- Import Information
- import
- Registration Date
- Jan 21, 1987
- Expiry Date
- Jan 21, 1992
- Cancellation Date
- Oct 07, 1999
- Status
- Logged out
- Reason
- 改列無須辦理查驗之醫療器材;;未展延而逾期者
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Access comprehensive regulatory information for Mah Respirator in Taiwan's medical device market through Pure Global AI's free database. is registered under number fdd1bc096bac4b093fadce0922fd28dc and manufactured by PENLON LTD.. The authorized representative in Taiwan is Sankyo Trading Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including KIMURA MEDICAL INSTRUMENT CO. LTD., MEGAMED AG ELECTRO-MEDINIZISCHE APPARATE, and 5 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.