"Leaf Clearer" Surgical Instruments, Motors & Accessories or Accessories (Unsterilized)
Taiwan·Risk Class 1·LEADM CORPORATION·Registered Oct 19, 2011 – Oct 19, 2016Cancelled- Analysis ID
- 5d13d45c9f50028920849b0a5aa909d3
- Customs Code
- DHA04401095508
- Manufacturer
- LEADM CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Fei Yan Biomedical Co., Ltd
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4820 Surgical Appliances and Accessories or Accessories
- Import Information
- import
- Registration Date
- Oct 19, 2011
- Expiry Date
- Oct 19, 2016
- Cancellation Date
- Jun 25, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Leaf Clearer" Surgical Instruments, Motors & Accessories or Accessories (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5d13d45c9f50028920849b0a5aa909d3 and manufactured by LEADM CORPORATION. The authorized representative in Taiwan is Fei Yan Biomedical Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LEADM CORPORATION, and 2 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.