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ETREBELLE - Indonesia BPOM Medical Device Registration

ETREBELLE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602126217. The device is manufactured by SPIRIT CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HAJU MEDICAL 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
ETREBELLE
Analysis ID: AKL 31602126217

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SPIRIT CO., LTD

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta

Registration Date

Mar 16, 2022

Expiry Date

Apr 12, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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