Taiwan FDA registration 9a01c2be2fee59d98eabbf35d2e1460a
“kitazato” OPU Needle
TW: “北里”取卵針
Taiwan·Risk Class 2·MD·Kitazato Corporation Tokyo office·Registered Nov 19, 2015 – Nov 19, 2020CancelledRegistration details
- Analysis ID
- 9a01c2be2fee59d98eabbf35d2e1460a
- License Form
- Ministry of Health Medical Device Import No. 027851
- Customs Code
- DHA05602785100
Company information
- Manufacturer
- Kitazato Corporation Tokyo office
- Manufacturer Country
- Japan
- Authorized Representative
- HONG-U SCENTIFIC CORP.
Product details
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L6100 Guide needle for assisted reproduction
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 19, 2015
- Expiry Date
- Nov 19, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “kitazato” OPU Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a01c2be2fee59d98eabbf35d2e1460a and manufactured by Kitazato Corporation Tokyo office. The authorized representative in Taiwan is HONG-U SCENTIFIC CORP..
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