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SINGFILLER Cross-linked Sodium Hyaluronate Gel - Indonesia BPOM Medical Device Registration

SINGFILLER Cross-linked Sodium Hyaluronate Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320329. The device is manufactured by HANGZHOU SINGCLEAN MEDICAL PRODUCTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PABLO GANESA FARMINDO.

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
SINGFILLER Cross-linked Sodium Hyaluronate Gel
Analysis ID: AKL 31602320329

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. PABLO GANESA FARMINDO

AR Address

JL.SEI SILAU KOMPLEK MEDAN BARU RESIDENCE NO.1, RT.000/RW.000

Registration Date

Jan 05, 2024

Expiry Date

Mar 13, 2025

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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