OLIGIO - Indonesia BPOM Medical Device Registration
OLIGIO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603121038. The device is manufactured by WON TECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRIME MED INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WON TECH CO., LTD.Country of Origin
Korea
Authorized Representative
PT. PRIME MED INDONESIAAR Address
Gedung MT Haryono Square Lt. 3, Unit 03 /5B Jl. Otto Iskandardinata No. 390, Kel. Bidaracina, Kec. Jatinegara, Jakarta Timur 13330
Registration Date
Feb 25, 2021
Expiry Date
Nov 16, 2023
Product Type
Surgical Equipment
Electrosurgical device for over-the-counter aesthetic use
Non Radiation Electromedics
V-Laser
Ultraskin Tightan II
Picocare 450
PICOCAREMAJESTY
OLIGIO
Oligio Kiss
WON TECH ULTRA SKIN II
LAVIEEN
PICOALEX
PASTELLE Laser, Surgical, Nd:YAG
WON TECH ULTRA SKIN II
WON TECH CO., LTD.
DAESHIN DS-40U (B)
DAESHIN ERTERPRISE CO., LTD.
DERMAV
LUTRONIC CORPORATION
CLARITY ™ LPY
LUTRONIC CORPORATION
INFINITE
LUTRONIC CORPORATION.
LASEMD Ultra
LUTRONIC CORPORATION
ACTION II
LUTRONIC CORPORATION.
eCO2 Plus
LUTRONIC CORPORATION.
SPECTRA XT
LUTRONIC CORPORATION.
HOLLYWOOD SPECTRA
LUTRONIC CORPORATION