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"Geelu" manually adjustable bed (unsterilized) - Taiwan Registration 308ada0764e5640d8ab1cc2afed8c82d

Access comprehensive regulatory information for "Geelu" manually adjustable bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 308ada0764e5640d8ab1cc2afed8c82d and manufactured by KUNSHAN KAWAZA MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is GENEMAX MEDICAL PRODUCTS INDUSTRY CORP..

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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308ada0764e5640d8ab1cc2afed8c82d
Registration Details
Taiwan FDA Registration: 308ada0764e5640d8ab1cc2afed8c82d
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Device Details

"Geelu" manually adjustable bed (unsterilized)
TW: "ๅ‰ๅพ‹" ๆ‰‹ๅ‹•ๅฏ่ชฟๆ•ดๅผ็—…ๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

308ada0764e5640d8ab1cc2afed8c82d

DHA04600180201

Company Information

Product Details

Limited to the first level of identification range of the Measures for the Administration of Medical Devices "Manual Adjustable Hospital Bed (J.5120)".

J General hospital and personal use equipment

J.5120 ๆ‰‹ๅ‹•ๅฏ่ชฟๆ•ดๅผ็—…ๅบŠ

Chinese goods;; input

Dates and Status

Nov 29, 2012

Nov 29, 2017

Dec 20, 2019

Cancellation Information

Logged out

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