Taiwan FDA registration 22840fea4da2fc7930ad7f20681f6e43
Pidi Safety Lancet (sterilization)
TW: 必帝 安全採血針(滅菌)
Taiwan·Risk Class 1·HTL-STREFA S.A.·Registered Mar 06, 2012 – Mar 06, 2027ActiveRegistration details
- Analysis ID
- 22840fea4da2fc7930ad7f20681f6e43
- Customs Code
- DHA04401143500
Company information
- Manufacturer
- HTL-STREFA S.A.
- Manufacturer Country
- Poland
- Authorized Representative
- BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 06, 2012
- Expiry Date
- Mar 06, 2027
About this record
Access comprehensive regulatory information for Pidi Safety Lancet (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 22840fea4da2fc7930ad7f20681f6e43 and manufactured by HTL-STREFA S.A.. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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