Taiwan FDA registration bcfa4de5656892a6d8fbd1eb98d450aa
"LDR" Manual surgical instrument for general use (Non-Sterile)
TW: "樂迪爾" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·LDR MEDICAL·Registered Mar 04, 2014 – Mar 04, 2019CancelledRegistration details
- Analysis ID
- bcfa4de5656892a6d8fbd1eb98d450aa
- License Form
- Ministry of Health Medical Device Import No. 013908
- Customs Code
- DHA09401390807
Company information
- Manufacturer
- LDR MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- HOLLING BIO-PHARMA. CORP.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2014
- Expiry Date
- Mar 04, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "LDR" Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bcfa4de5656892a6d8fbd1eb98d450aa and manufactured by LDR MEDICAL. The authorized representative in Taiwan is HOLLING BIO-PHARMA. CORP..
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