Taiwan FDA registration 3837f80f8f01a86b91606c89c4d3b2ee
“Myelotec” Flexible Fiberoptic Endoscope & Access Kits
TW: “麥洛泰克”軟式光纖內視鏡及其附件
Taiwan·Risk Class 2·MD·MYELOTEC, INC.·Registered Aug 01, 2013 – Aug 01, 2018CancelledRegistration details
- Analysis ID
- 3837f80f8f01a86b91606c89c4d3b2ee
- License Form
- Ministry of Health Medical Device Import No. 025315
- Customs Code
- DHA05602531502
Company information
- Manufacturer
- MYELOTEC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 01, 2013
- Expiry Date
- Aug 01, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Myelotec” Flexible Fiberoptic Endoscope & Access Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3837f80f8f01a86b91606c89c4d3b2ee and manufactured by MYELOTEC, INC.. The authorized representative in Taiwan is REVO LASER CORPORATION.
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