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METOOFILL+ POINT VOLUME Lidocaine - Indonesia BPOM Medical Device Registration

METOOFILL+ POINT VOLUME Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420127. 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. STAR COSPHARM INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
METOOFILL+ POINT VOLUME Lidocaine
Analysis ID: AKL 31602420127

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOPLUS CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. STAR COSPHARM INDONESIA

AR Address

Gedung Tifa Lantai 4 Suite 405A, Jl. Kuningan Barat 1 No. 26 RT.6/RW.1

Registration Date

Oct 10, 2024

Expiry Date

May 03, 2029

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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