Taiwan FDA registration 7980c3fefbf66093dc285992329f924d
"Gaist" ENT Manual Surgical Instruments (Unsterilized)
TW: "蓋司特" 耳鼻喉手動式外科器械 (未滅菌)
Taiwan·Risk Class 1·G. ALBERT STORZ·Registered Apr 13, 2006 – Apr 13, 2011CancelledRegistration details
- Analysis ID
- 7980c3fefbf66093dc285992329f924d
- Customs Code
- DHA04400373108
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 Science
- Product Type (Level 2)
- G.4420 Otolaryngology manual surgical instruments
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2006
- Expiry Date
- Apr 13, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gaist" ENT Manual Surgical Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7980c3fefbf66093dc285992329f924d 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