“FERNO” BACKBOARD STRETCHER (Non-Sterile)
Taiwan·Risk Class 1·MD·FERNO-WASHINGTON, INC.·Registered Oct 01, 2021 – Oct 31, 2024Expired- Analysis ID
- b1d8cca986ee5d7b4e2531ba7e65274f
- License Form
- Ministry of Health Medical Device Import Registration No. 014295
- Customs Code
- DHA08401429509
- Manufacturer
- FERNO-WASHINGTON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GOODMED CO., LTD.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Portable Stretcher (J.6900)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6900 portable stretcher
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
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Access comprehensive regulatory information for “FERNO” BACKBOARD STRETCHER (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1d8cca986ee5d7b4e2531ba7e65274f and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is GOODMED CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FERNO-WASHINGTON, INC., and 3 recent registrations in the same category. 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.