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REVANESSE ULTRA+ - Indonesia BPOM Medical Device Registration

REVANESSE ULTRA+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220093. The device is manufactured by PROLLENIUM MEDICAL TECHNOLOGIES INC. from Canada, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MENJANGAN SAKTI.

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
REVANESSE ULTRA+
Analysis ID: AKL 31602220093

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Canada

Authorized Representative

PT. MENJANGAN SAKTI

AR Address

Jl. HR. Rasuna Said Kav. B-34 Kuningan

Registration Date

Sep 28, 2022

Expiry Date

Jul 07, 2024

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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