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VIVABELLA - Indonesia BPOM Medical Device Registration

VIVABELLA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320199. 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 SMELL 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
VIVABELLA
Analysis ID: AKL 31602320199

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SPIRIT CO., LTD

Country of Origin

Korea

Authorized Representative

SMELL 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

May 30, 2023

Expiry Date

Oct 31, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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