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"Bausch & Len" Ophthalmic Manual Device (Unsterilized) - Taiwan Registration 8d051417dd5cd221a0148afbbeeac4ef

Access comprehensive regulatory information for "Bausch & Len" Ophthalmic Manual Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8d051417dd5cd221a0148afbbeeac4ef and manufactured by BAUSCH & LOMB GMBH. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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8d051417dd5cd221a0148afbbeeac4ef
Registration Details
Taiwan FDA Registration: 8d051417dd5cd221a0148afbbeeac4ef
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Device Details

"Bausch & Len" Ophthalmic Manual Device (Unsterilized)
TW: โ€œๅšๅฃซๅ€ซโ€่ฆ–ๅฐŽ็œผ็ง‘ๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8d051417dd5cd221a0148afbbeeac4ef

DHA04400552005

Company Information

Germany

Product Details

Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Jan 11, 2007

Jan 11, 2027