Taiwan FDA registration cfeff7cc90503dafbd7512c2c3fe2595
"Etac" Non-AC-powered Patient lift (Non-sterile)
TW: "益他" 非交流電力式病患升降機 (未滅菌)
Registration details
- Analysis ID
- cfeff7cc90503dafbd7512c2c3fe2595
- License Form
- Ministry of Health Medical Device Import No. 017758
- Customs Code
- DHA09401775808
Company information
- Manufacturer
- Etac AS,Etac Supply Gjovik
- Manufacturer Country
- Norway
- 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
- Apr 25, 2017
- Expiry Date
- Apr 25, 2022
About this record
Access comprehensive regulatory information for "Etac" 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 cfeff7cc90503dafbd7512c2c3fe2595 and manufactured by Etac AS,Etac Supply Gjovik. 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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