Taiwan FDA registration 4686c005030a529110ca1aec63f4dec0
“OLYMPUS” Single Use Grasping Forceps
TW: “奧林柏斯”單次用異物鉗
Registration details
- Analysis ID
- 4686c005030a529110ca1aec63f4dec0
- License Form
- Ministry of Health Medical Device Import No. 034599
- Customs Code
- DHA05603459904
Company information
- Manufacturer
- AOMORI OLYMPUS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jun 18, 2021
- Expiry Date
- Jun 18, 2026
About this record
Access comprehensive regulatory information for “OLYMPUS” Single Use Grasping Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4686c005030a529110ca1aec63f4dec0 and manufactured by AOMORI OLYMPUS CO., LTD.. 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