Taiwan FDA registration 00d1dc247c803b3c381c00b529f809d8
"Guinici" Demei Gene dermabrasion machine (unsterilized)
TW: “紀妮希” 德美基因 磨皮機 (未滅菌)
Taiwan·Risk Class 1·GENESIS BIOSYSTEMS, INC.·Registered Jan 24, 2013 – Jan 24, 2018CancelledRegistration details
- Analysis ID
- 00d1dc247c803b3c381c00b529f809d8
- Customs Code
- DHA04401263806
Company information
- Manufacturer
- GENESIS BIOSYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Wo Medical Limited
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4820 Surgical Appliances and Accessories or Accessories
- Import Information
- import
Dates and status
- Registration Date
- Jan 24, 2013
- Expiry Date
- Jan 24, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Guinici" Demei Gene dermabrasion machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 00d1dc247c803b3c381c00b529f809d8 and manufactured by GENESIS BIOSYSTEMS, INC.. The authorized representative in Taiwan is Wo Medical Limited.
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