Taiwan FDA registration dd0871f642f0013e3216ffe0da6dc8ad
"Luther" orthopedic manual arthroscopic equipment (unsterilized)
TW: “路德”骨科手動式關節鏡器材(未滅菌)
Taiwan·Risk Class 1·LUT GMBH·Registered Jul 03, 2009 – Jul 03, 2014CancelledRegistration details
- Analysis ID
- dd0871f642f0013e3216ffe0da6dc8ad
- Customs Code
- DHA04400788401
Company information
- Manufacturer
- LUT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.1100 Closing Lenses
- Import Information
- import
Dates and status
- Registration Date
- Jul 03, 2009
- Expiry Date
- Jul 03, 2014
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Luther" orthopedic manual arthroscopic equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd0871f642f0013e3216ffe0da6dc8ad and manufactured by LUT GMBH. The authorized representative in Taiwan is REVO LASER CORPORATION.
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