Taiwan FDA registration 3d8fea8db6e1c0b6ff8a43d7bed1668b
“OLYMPUS” Single Use Aspiration Needle NA-U403SX
TW: “奧林柏斯”單次使用抽吸生檢針
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered Feb 18, 2021 – Feb 18, 2026ExpiredRegistration details
- Analysis ID
- 3d8fea8db6e1c0b6ff8a43d7bed1668b
- License Form
- Ministry of Health Medical Device Import No. 034289
- Customs Code
- DHA05603428902
Company information
- Manufacturer
- Gyrus ACMI, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4680 Bronchoscope (soft or rigid) and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 18, 2021
- Expiry Date
- Feb 18, 2026
About this record
Access comprehensive regulatory information for “OLYMPUS” Single Use Aspiration Needle NA-U403SX in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3d8fea8db6e1c0b6ff8a43d7bed1668b and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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