Laser Treatment Device
Vietnam·Risk Class TTBYT Loại B·Lumix® 2; Lumix®CPS; Lumix® CW; Lumix® Ultra; Lumix® 100; Lumix® 250·Fisioline S.r.l.·Registered Jun 10, 2022- Analysis ID
- 220001999/PCBB-HN
- Submission ID
- 000.00.19.H26-220601-0004
- Product Type
- Lumix® 2; Lumix®CPS; Lumix® CW; Lumix® Ultra; Lumix® 100; Lumix® 250
- Manufacturer
- Fisioline S.r.l.
- Intended Use
- Used in physical therapy, functional recovery
- Registration Date
- Jun 10, 2022
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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..
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