Laser Treatment Machine
Vietnam·Risk Class TTBYT Loại B·Lumix C.P.S., Lumix CW, Lumix Plus, Lumix Ultra, Lumix Q, Lumix 100, Lumix 250, Lumix 2·Fisioline srl·Registered Aug 23, 2024- Analysis ID
- 240002110/PCBB-HN
- Submission ID
- 000.00.19.H26-220330-0004
- Product Type
- Lumix C.P.S., Lumix CW, Lumix Plus, Lumix Ultra, Lumix Q, Lumix 100, Lumix 250, Lumix 2
- Manufacturer
- Fisioline srl
- Product Owner
- Fisioline srl
- Authorized Representative
- CÔNG TY TNHH XUẤT NHẬP KHẨU THIẾT BỊ THÁI VIỆT
- Intended Use
- Distribution
- Registration Date
- Aug 23, 2024
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Access comprehensive regulatory information for Laser Treatment Machine 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 240002110/PCBB-HN and manufactured by Fisioline srl. The authorized representative in Vietnam is CÔNG TY TNHH XUẤT NHẬP KHẨU THIẾT BỊ THÁI VIỆT.
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including EME S.R.L., EME, 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.