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INSTAR S1 with Lidocaine - Indonesia BPOM Medical Device Registration

INSTAR S1 with Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320188. The device is manufactured by BIOPLUS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SUCCESS WITH DAVID.

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BPOM Registered
Risk Class Kelas Resiko : D
INSTAR S1 with Lidocaine
Analysis ID: AKL 31602320188

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOPLUS CO., LTD

Country of Origin

Korea

Authorized Representative

PT. SUCCESS WITH DAVID

AR Address

Gedung Nucira Lt. 3, Jl. MT. Haryono Kav. 27, Tebet Timur, Tebet

Registration Date

Apr 27, 2023

Expiry Date

Aug 21, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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