Taiwan FDA registration 9a59704d131fb5c850be02d7224b2e64
"Lester" ENT manual surgical instruments (unsterilized)
TW: "雷斯特" 耳鼻喉手動式外科器械(未滅菌)
Taiwan·Risk Class 1·RUDOLF RIESTER GMBH·Registered Feb 25, 2011 – Feb 25, 2021CancelledRegistration details
- Analysis ID
- 9a59704d131fb5c850be02d7224b2e64
- Customs Code
- DHA04400994709
Company information
- Manufacturer
- RUDOLF RIESTER GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- FU TAI TRADING CO., LTD.
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
- Feb 25, 2011
- Expiry Date
- Feb 25, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lester" 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 9a59704d131fb5c850be02d7224b2e64 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is FU TAI TRADING 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