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"Marco" cantilever system (non-sterile) - Taiwan Registration b92c8d4b6c6e17a9e680839342b497f9

Access comprehensive regulatory information for "Marco" cantilever system (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 b92c8d4b6c6e17a9e680839342b497f9 and manufactured by KLS Martin SE & Co. KG;; KLS Martin SE & Co.KG. The authorized representative in Taiwan is KINDMED CORPORATION.

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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b92c8d4b6c6e17a9e680839342b497f9
Registration Details
Taiwan FDA Registration: b92c8d4b6c6e17a9e680839342b497f9
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Device Details

"Marco" cantilever system (non-sterile)
TW: "็‘ช็ฝ" ๆ‡ธ่‡‚็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b92c8d4b6c6e17a9e680839342b497f9

DHA09402360903

Company Information

Product Details

It is limited to the first level of identification of the "Electric or Pneumatic Surgical Operating Tables, Surgical Chairs and Their Accessories (I.4960)" of the Measures for the Classification and Grading of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4960 Electric or pneumatic surgical tables, surgical chairs, and accessories thereof

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Sep 20, 2024

Sep 20, 2029