"Kaneta" Manual patient transfer device (Non-Sterile)
Taiwan·Risk Class 1·MD·KANETA CORPORATION INC.·Registered Sep 18, 2017 – Sep 18, 2022Cancelled- Analysis ID
- 4a02358f0c0b24c0b9a306b0407fcbd8
- License Form
- Ministry of Health Medical Device Import No. 018317
- Customs Code
- DHA09401831709
- Manufacturer
- KANETA CORPORATION INC.
- Manufacturer Country
- Japan
- Authorized Representative
- ABILITIES HEALTHCARE INCORPORATED
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J6785 Manual Patient Conveyor
- Import Information
- Imported from abroad
- Registration Date
- Sep 18, 2017
- Expiry Date
- Sep 18, 2022
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Kaneta" Manual patient transfer device (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 4a02358f0c0b24c0b9a306b0407fcbd8 and manufactured by KANETA CORPORATION INC.. The authorized representative in Taiwan is ABILITIES HEALTHCARE INCORPORATED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KANETA CORPORATION INC., and 1 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.