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Beads Max Mid Lidocaine - Indonesia BPOM Medical Device Registration

Beads Max Mid Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320182. 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. GREAT PERFECT UNIVERSE.

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
Beads Max Mid Lidocaine
Analysis ID: AKL 31602320182

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIOPLUS CO.,LTD

Country of Origin

Korea

Authorized Representative

PT. GREAT PERFECT UNIVERSE

AR Address

AGUNG SEMPURNA SEMESTA

Registration Date

Apr 18, 2023

Expiry Date

Sep 07, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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