Taiwan FDA registration 13b29a13047f7fc656f7ad2bc3121759
Red head fixture
TW: 雷德頭部固定裝具
Taiwan·Risk Class 1·LAERDAL MEDICAL AS·Registered Mar 31, 2006 – Mar 31, 2011CancelledRegistration details
- Analysis ID
- 13b29a13047f7fc656f7ad2bc3121759
- Customs Code
- DHA04400338808
Company information
- Manufacturer
- LAERDAL MEDICAL AS
- Manufacturer Country
- Norway
- Authorized Representative
- Xin Yi Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices (Torso Equipment [O.3490]).
- Product Type (Level 1)
- o Physical Medical Sciences
- Import Information
- import
Dates and status
- Registration Date
- Mar 31, 2006
- Expiry Date
- Mar 31, 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 Red head fixture in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13b29a13047f7fc656f7ad2bc3121759 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xin Yi Limited.
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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