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SYNOVIAL 0.8% - Indonesia BPOM Medical Device Registration

SYNOVIAL 0.8% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302710597. The device is manufactured by IBSA FARMACEUTICI ITALIA SRL. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. GRACE ARGON MEDICA.

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
SYNOVIAL 0.8%

SINOVIAL 0.8%

Analysis ID: AKL 31302710597

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Italy

Authorized Representative

PT. GRACE ARGON MEDICA

AR Address

Titan Center, Lantai 4 Jl. Boulevard Bintaro Block B7/B1 No.05 Bintaro Jaya Sector 7

Registration Date

Oct 08, 2023

Expiry Date

Jan 29, 2026

Product Type

Prosthetic Orthopedic Equipment

Intra articular fluid

Non Electromedic Sterile

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