Taiwan FDA registration 2b0e427eefc028ce1fba4ef37317b4e1
Ceralas HPD Laser System
TW: 薩爾拉斯雷射儀
Taiwan·Risk Class 2·MD·CeramOptec GmbH·Registered Dec 12, 2017 – Dec 12, 2022ExpiredRegistration details
- Analysis ID
- 2b0e427eefc028ce1fba4ef37317b4e1
- License Form
- Ministry of Health Medical Device Import No. 030592
- Customs Code
- DHA05603059209
Company information
- Manufacturer
- CeramOptec GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- ANDERSON MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2017
- Expiry Date
- Dec 12, 2022
About this record
Access comprehensive regulatory information for Ceralas HPD Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b0e427eefc028ce1fba4ef37317b4e1 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY 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