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PERFECTHA DERM LIDOCAINE - Indonesia BPOM Medical Device Registration

PERFECTHA DERM LIDOCAINE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320170. The device is manufactured by SINCLAIR FRANCE SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BINASUKSES CANTEEN.

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BPOM Registered
Risk Class Kelas Resiko : D
PERFECTHA DERM LIDOCAINE
Analysis ID: AKL 31602320170

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

France

Authorized Representative

PT. BINASUKSES CANTEEN

AR Address

JL. PULO KAMBING II NO.26 KAWASAN INDUSTRI PULOGADUNG

Registration Date

Mar 30, 2023

Expiry Date

May 26, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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