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DORNIER Thulio - Indonesia BPOM Medical Device Registration

DORNIER Thulio is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324901. The device is manufactured by DORNIER MEDTECH GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOMEDIK NIAGA PERKASA.

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BPOM Registered
Risk Class Kelas Resiko : C
DORNIER Thulio
Analysis ID: AKL 21603324901

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

INDOMEDIK NIAGA PERKASA

AR Address

Jl. Raya Kebayoran Lama No.35 RT.008 RW.001 Kelurahan Sukabumi Selatan, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

Sep 05, 2023

Expiry Date

Mar 31, 2027

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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