Taiwan FDA registration 129b06fdd2c810d3e86b4137b71b31ee
"Pine" alternating decompression air bed (unsterilized)
TW: “松柏”交替式減壓氣墊床 (未滅菌)
Taiwan·Risk Class 1·Pine Cypress Medical Instrument Co., Ltd·Registered Dec 06, 2007 – Dec 06, 2012CancelledRegistration details
- Analysis ID
- 129b06fdd2c810d3e86b4137b71b31ee
Company information
- Manufacturer
- Pine Cypress Medical Instrument Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Pine Cypress Medical Instrument Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5550 交替式壓力氣墊床
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 06, 2007
- Expiry Date
- Dec 06, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pine" alternating decompression air bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 129b06fdd2c810d3e86b4137b71b31ee and manufactured by Pine Cypress Medical Instrument Co., Ltd. The authorized representative in Taiwan is Pine Cypress Medical Instrument Co., Ltd.
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