DIOLAS Newton One Diode Laser - Indonesia BPOM Medical Device Registration
DIOLAS Newton One Diode Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603423002. The device is manufactured by LIMMER LASER GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LIMMER LASER GMBHCountry of Origin
Germany
Authorized Representative
PT. SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530
Registration Date
Dec 30, 2024
Expiry Date
Jul 22, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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