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Laser Treatment Device - Vietnam Registration 220001999/PCBB-HN

Access comprehensive regulatory information for Laser Treatment Device in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 220001999/PCBB-HN and manufactured by Fisioline S.r.l..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including ILOODA CO.,LTD, ILOODA Co., Ltd, and 5 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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220001999/PCBB-HN
Registration Details
Vietnam MOH Registration: 220001999/PCBB-HN
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Device Details

Laser Treatment Device
VN: Thiết bị Laser điều trị
Risk Class TTBYT Loại B

Registration Details

220001999/PCBB-HN

000.00.19.H26-220601-0004

Lumix® 2; Lumix®CPS; Lumix® CW; Lumix® Ultra; Lumix® 100; Lumix® 250

Company Information

Technical Details

Used in physical therapy, functional recovery

Dates and Status

Jun 10, 2022