Taiwan FDA registration 091935e0413e23e824daeb99704366af
"Solo step" Non-AC-powered Patient lift (Non-sterile)
TW: "不倒翁"非交流電力式病患升降機 (未滅菌)
Registration details
- Analysis ID
- 091935e0413e23e824daeb99704366af
- License Form
- Ministry of Health Medical Device Import No. 021163
- Customs Code
- DHA09402116305
Company information
- Manufacturer
- SOLOSTEP INC.
- Manufacturer Country
- United States
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5510 Non-AC Electric Patient Lift
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 06, 2020
- Expiry Date
- Jan 06, 2025
About this record
Access comprehensive regulatory information for "Solo step" Non-AC-powered Patient lift (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 091935e0413e23e824daeb99704366af and manufactured by SOLOSTEP INC.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
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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