Taiwan FDA registration 23174c4e4f2465ebf4ebca22782bafb5

Components for extracorporeal limb equipment (unsterilized)

TW: “重維歐恩比”體外肢體裝具用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Heavy Maintenance Rehabilitation Products Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
23174c4e4f2465ebf4ebca22782bafb5
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the classification and grading management methods of medical equipment, in vitro limb equipment components (O.3410) the first level identification range.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3410 體外肢體裝具用組件
Import Information
Domestic
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for Components for extracorporeal limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23174c4e4f2465ebf4ebca22782bafb5 and manufactured by Heavy Maintenance Rehabilitation Products Co., Ltd. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Heavy Maintenance Rehabilitation Products Co., Ltd, 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.

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