Taiwan FDA registration 37f143d2e8bd7315abc23f4da92b78ad
Operak tear duct plug
TW: 歐沛拉克淚管塞
Registration details
- Analysis ID
- 37f143d2e8bd7315abc23f4da92b78ad
- Customs Code
- DHA00601983905
Company information
- Manufacturer
- LACRIMEDICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kangcheng Biomedical Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2009
- Expiry Date
- May 12, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Operak tear duct plug in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37f143d2e8bd7315abc23f4da92b78ad and manufactured by LACRIMEDICS INC.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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