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Bausch + Lomb Ultra One Day (Kalifilcon A) Soft Contact Lens - Taiwan Registration 1c46d67b022040efa6705bfc0ca0fc6f

Access comprehensive regulatory information for Bausch + Lomb Ultra One Day (Kalifilcon A) Soft Contact Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c46d67b022040efa6705bfc0ca0fc6f and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bausch & Lomb Incorporated, and 1 recent registrations in the same category. 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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1c46d67b022040efa6705bfc0ca0fc6f
Registration Details
Taiwan FDA Registration: 1c46d67b022040efa6705bfc0ca0fc6f
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Device Details

Bausch + Lomb Ultra One Day (Kalifilcon A) Soft Contact Lens
TW: ๅšๅฃซๅ€ซ่ผ•ๆฐดๆฐงๅฅงๆพˆ็Ÿฝๆฐด่† ๆ—ฅๆ‹‹้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

1c46d67b022040efa6705bfc0ca0fc6f

Ministry of Health Medical Device Import No. 034041

DHA05603404105

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M5925 Flexible Contact Lens

Imported from abroad

Dates and Status

Apr 14, 2021

Apr 14, 2026

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