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"Vella" IOL guide (sterilization) - Taiwan Registration ee8bdeb6bc6b0218915bee2b8856205b

Access comprehensive regulatory information for "Vella" IOL guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ee8bdeb6bc6b0218915bee2b8856205b and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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ee8bdeb6bc6b0218915bee2b8856205b
Registration Details
Taiwan FDA Registration: ee8bdeb6bc6b0218915bee2b8856205b
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Device Details

"Vella" IOL guide (sterilization)
TW: โ€œๅจๆœ—โ€ ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ee8bdeb6bc6b0218915bee2b8856205b

DHA09401810201

Company Information

Poland

Product Details

Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

Input;; QMS/QSD

Dates and Status

Jul 24, 2017

Jul 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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