"Nipro" blood lancet (sterilized)
Taiwan·Risk Class 1·NIPRO DIAGNOSTICS, INC.;; Tianjin Huahong Technology Co., Ltd.·Registered Jul 02, 2013 – Jul 02, 2018Cancelled- Analysis ID
- f0916cbc6be7c737745f923e6f756f00
- Customs Code
- DHA04600192402
- Manufacturer Country
- United States;;China
- Authorized Representative
- Taiwan Nipro Medical Device Co., Ltd
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; Contract manufacturing;; Input;; Chinese goods
- Registration Date
- Jul 02, 2013
- Expiry Date
- Jul 02, 2018
- Cancellation Date
- May 19, 2022
- Status
- Logged out
- Reason
- 自行鍵入
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Access comprehensive regulatory information for "Nipro" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f0916cbc6be7c737745f923e6f756f00 and manufactured by NIPRO DIAGNOSTICS, INC.;; Tianjin Huahong Technology Co., Ltd.. The authorized representative in Taiwan is Taiwan Nipro Medical Device Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Tianjin Huahong Technology 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.