Taiwan FDA registration f7b27d212784da7c521d188cb21fdf4d
"ALBERT" Ear, Nose, and Throat manual surgical instrument (Non-Sterile)
TW: "亞爾伯" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·MD·G. ALBERT STORZ·Registered Mar 27, 2017 – Mar 27, 2022ExpiredRegistration details
- Analysis ID
- f7b27d212784da7c521d188cb21fdf4d
- License Form
- Ministry of Health Medical Device Import No. 017646
- Customs Code
- DHA09401764600
Company information
- Manufacturer
- G. ALBERT STORZ
- Manufacturer Country
- Germany
- Authorized Representative
- PRIMA SURGICAL COMPANY
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4420 OTOLARYNGARY Manual Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 27, 2017
- Expiry Date
- Mar 27, 2022
About this record
Access comprehensive regulatory information for "ALBERT" Ear, Nose, and Throat manual surgical instrument (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 f7b27d212784da7c521d188cb21fdf4d and manufactured by G. ALBERT STORZ. The authorized representative in Taiwan is PRIMA SURGICAL COMPANY.
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