SDI – Gingival Barrier - Indonesia BPOM Medical Device Registration
SDI – Gingival Barrier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605023656. The device is manufactured by SDI LIMITED from Australia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is LABORA MANDIRI INDO PRATAMA.
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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
SDI LIMITEDCountry of Origin
Australia
Authorized Representative
LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Oct 07, 2022
Expiry Date
Jul 01, 2025
Product Type
Other Dental Equipment
Rubber dam and accessories.
Non Electromedic Non Sterile
SDI – Stela Automix Intro Kit
SDI – Riva Cem Automix
SDI – Pola Office
SDI – Riva Star
SDI – Poladay CP
SDI – Moon
SDI – Aura Easy
SDI – Aura Easyflow
SDI - Set PP
SDI – Aura Bulk Fill
STERILERIGHT – Sterilization Flat Rolls
STERILERIGHT PACKAGING MFG INC.
CAVEX – ProphyPaste
CAVEX HOLLAND B.V
CAVEX – Bite & White Shade Correction
CAVEX HOLLAND B.V.
RUSCH – Valve Integral Ureter Stent Set Wiruthan
ARROW INTERNATIONAL CR A.S.
RUSCH – Superglide Valve DD Ureter Stent Set Wiruthan
ARROW INTERNATIONAL CR A.S.
MEDISPONGE – Absorbable Haemostatic Gelatin Sponge
AEGIS LIFESCIENCES PVT., LTD
MAICO – Easytone
DGS DIAGNOSTICS SP. Z.O.O
HEINE Mini 3000 F.O. Otoscope
HEINE OPTOTECHNIK GMBH & CO. KG
FOREMOUNT – Disposable Manual Resuscitator
FOREMOUNT ENTERPRISE CO., LTD
HEINE Mini 3000 Otoscope
HEINE OPTOTECHNIK GMBH & CO. KG.