Taiwan FDA registration 294897d2e5e388fe156c2dfd514eebac
"Donglin potentiometer"
TW: "東林"電位治療器
Taiwan·Risk Class 2·Lacoli GmbH·Registered Nov 15, 2006 – Nov 15, 2011CancelledRegistration details
- Analysis ID
- 294897d2e5e388fe156c2dfd514eebac
- Customs Code
- DHY00500209302
Company information
- Manufacturer
- Lacoli GmbH
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- COMLINK ELECTRONIC CO., LTD.
Product details
- Intended Use
- Relieves stiff shoulders, headaches, chronic constipation.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.0001 靜電器(電位治療器)
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Nov 15, 2006
- Expiry Date
- Nov 15, 2011
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Donglin potentiometer" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 294897d2e5e388fe156c2dfd514eebac and manufactured by Lacoli GmbH. The authorized representative in Taiwan is COMLINK ELECTRONIC 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.
Free DatabasePowered by Pure Global AI89,000+ Devices