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ZEISS Henfrey Vision Analyzer II-I Series (Unsterilized) - Taiwan Registration b313c721dc57162eaaa7ee90d034b39d

Access comprehensive regulatory information for ZEISS Henfrey Vision Analyzer II-I Series (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b313c721dc57162eaaa7ee90d034b39d and manufactured by CARL ZEISS MEDITEC, INC.. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

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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b313c721dc57162eaaa7ee90d034b39d
Registration Details
Taiwan FDA Registration: b313c721dc57162eaaa7ee90d034b39d
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Device Details

ZEISS Henfrey Vision Analyzer II-I Series (Unsterilized)
TW: ่”กๅธ้Ÿ“็ฆ็‘ž่ฆ–้‡Žๅˆ†ๆžๅ„€II-I็ณปๅˆ— (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b313c721dc57162eaaa7ee90d034b39d

DHA04400096607

Company Information

United States

Product Details

Used to check the extent of the patient's peripheral vision. The device casts different points of light on the surface and allows the patient to indicate whether they can see the light or not.

M Ophthalmology

M.1605 Periscope

import

Dates and Status

Oct 17, 2005

Oct 17, 2020

Jun 07, 2022

Cancellation Information

Logged out

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