Taiwan FDA registration 765b6485379774d0aeb71a61c9d36c55
Pentax Manual Instruments for Surgery (Unsterilized)
TW: “賓得士”手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·PENTAX CORPORATION·Registered May 04, 2006 – May 04, 2011CancelledRegistration details
- Analysis ID
- 765b6485379774d0aeb71a61c9d36c55
- Customs Code
- DHA04400433801
Company information
- Manufacturer
- PENTAX CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- May 04, 2006
- Expiry Date
- May 04, 2011
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Pentax Manual Instruments for Surgery (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 765b6485379774d0aeb71a61c9d36c55 and manufactured by PENTAX CORPORATION. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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