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Pupillary manual refractive needle (unsterilized) - Taiwan Registration 691338c89837b7bc87935a7b173ca76e

Access comprehensive regulatory information for Pupillary manual refractive needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 691338c89837b7bc87935a7b173ca76e and manufactured by SHANGHAI HUVITZ CO., LTD.. The authorized representative in Taiwan is Mingda Development Company Limited.

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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691338c89837b7bc87935a7b173ca76e
Registration Details
Taiwan FDA Registration: 691338c89837b7bc87935a7b173ca76e
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Device Details

Pupillary manual refractive needle (unsterilized)
TW: ็žณๅ…‰ๆ‰‹ๅ‹•ๆŠ˜ๅฐ„้‡(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

691338c89837b7bc87935a7b173ca76e

DHA04600164702

Company Information

China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Refractometer (M.1770)".

M Ophthalmology

M.1770 ๆ‰‹ๅ‹•ๅผ้ฉ—ๅ…‰ๅ„€

QMS/QSD;; Input;; Chinese goods

Dates and Status

May 29, 2012

May 29, 2017

Nov 29, 2017

Cancellation Information

Logged out

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