Taiwan FDA registration 2cd7390a5f5c79c4679c1729442f6d3a

Matilda components for in vitro limb prosthetics (unsterilized)

TW: "明德" 體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Wande Disabled Equipment Co., Ltd. Zhonghe Factory;; Mentor Medical Assistive Devices Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
2cd7390a5f5c79c4679c1729442f6d3a
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MINGDER MEDICAL ORTHOTICS CO.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3420 體外肢體義肢用組件
Import Information
Domestic;; Contract manufacturing
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 Matilda components for in vitro limb prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2cd7390a5f5c79c4679c1729442f6d3a and manufactured by Wande Disabled Equipment Co., Ltd. Zhonghe Factory;; Mentor Medical Assistive Devices Co., Ltd. The authorized representative in Taiwan is MINGDER MEDICAL ORTHOTICS CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Wande Disabled Equipment Co., Ltd. Zhonghe Factory, 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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