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"Bidi" ophthalmic catheters and peripheral accessories - Taiwan Registration 42377d27658151534016e1682da4714d

Access comprehensive regulatory information for "Bidi" ophthalmic catheters and peripheral accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42377d27658151534016e1682da4714d and manufactured by BD OPHTHALMIC SYSTEMS. The authorized representative in Taiwan is Taiwan Branch of American Business Bidi 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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42377d27658151534016e1682da4714d
Registration Details
Taiwan FDA Registration: 42377d27658151534016e1682da4714d
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Device Details

"Bidi" ophthalmic catheters and peripheral accessories
TW: "ๅฟ…ๅธ" ็œผ็”จๅฐŽ็ฎกๅŠ้€ฑ้‚Š้…ไปถ
Risk Class 1
Cancelled

Registration Details

42377d27658151534016e1682da4714d

DHA04400270301

Company Information

United Kingdom

Product Details

Non-electric, hand-held devices used to assist or perform eye surgery.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Feb 22, 2006

Feb 22, 2011

Jun 10, 2011

Cancellation Information

Logged out

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