Taiwan FDA registration 1f09b4d4a4857a129db9073664c3eeb0
"New Japan" Sight Lantern Machine (unsterilized)
TW: "新日本" 視力幻燈機 (未滅菌)
Registration details
- Analysis ID
- 1f09b4d4a4857a129db9073664c3eeb0
- Customs Code
- DHA04400246702
Company information
- Manufacturer
- TOWA MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Synergy Optics Ltd
Product details
- Intended Use
- It is an alternating current electrical device used to project visual and sensory images on a screen.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1680 眼科用投影機
- Import Information
- import
Dates and status
- Registration Date
- Jan 05, 2006
- Expiry Date
- Jan 05, 2011
- Cancellation Date
- May 19, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "New Japan" Sight Lantern 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 1f09b4d4a4857a129db9073664c3eeb0 and manufactured by TOWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Synergy Optics Ltd.
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