Taiwan FDA registration 60d5f80909323c68ec9fa5d7ef9f19de
“MANI” SURGICAL EYED NEEDLES (Non-sterile)
TW: “馬尼”外科用縫合針 (未滅菌)
Taiwan·Risk Class 1·MD·MANI HANOI CO., LTD.·Registered Mar 11, 2019 – Mar 11, 2024ExpiredRegistration details
- Analysis ID
- 60d5f80909323c68ec9fa5d7ef9f19de
- License Form
- Ministry of Health Medical Device Import No. 020162
- Customs Code
- DHA09402016201
Company information
- Manufacturer
- MANI HANOI CO., LTD.
- Manufacturer Country
- Viet Nam
- Authorized Representative
- UNIK SURGICAL SUTURES MFG. CO.
Product details
- 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 and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 11, 2019
- Expiry Date
- Mar 11, 2024
About this record
Access comprehensive regulatory information for “MANI” SURGICAL EYED NEEDLES (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 60d5f80909323c68ec9fa5d7ef9f19de and manufactured by MANI HANOI CO., LTD.. The authorized representative in Taiwan is UNIK SURGICAL SUTURES MFG. CO..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices