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REMEDIUM PLUS FINE - Indonesia BPOM Medical Device Registration

REMEDIUM PLUS FINE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320291. The device is manufactured by BIO PLUS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PRIME NATURAL CHARM.

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
REMEDIUM PLUS FINE
Analysis ID: AKL 31602320291

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BIO PLUS CO., LTD

Country of Origin

Korea

Authorized Representative

PT. PRIME NATURAL CHARM

AR Address

PRIMA PESONA ALAMI

Registration Date

Oct 25, 2023

Expiry Date

Mar 31, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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