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Bausch + Lomb ReNu Fresh Multi-Purpose Solution - Taiwan Registration e0ac5b194a8a0b40312eb70550065550

Access comprehensive regulatory information for Bausch + Lomb ReNu Fresh Multi-Purpose Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e0ac5b194a8a0b40312eb70550065550 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. 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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e0ac5b194a8a0b40312eb70550065550
Registration Details
Taiwan FDA Registration: e0ac5b194a8a0b40312eb70550065550
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Device Details

Bausch + Lomb ReNu Fresh Multi-Purpose Solution
TW: ๅšๅฃซๅ€ซ็‘ž้œ–็‚ซ่Œๅคšๆ•ˆไฟ้คŠๆถฒ
Risk Class 2
MD

Registration Details

e0ac5b194a8a0b40312eb70550065550

Ministry of Health Medical Device Import No. 027308

DHA05602730802

Company Information

United States

Product Details

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

M Ophthalmic devices

M5928 Flexible Contact Lens Preservation

Imported from abroad

Dates and Status

May 28, 2015

Oct 22, 2025