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REBSCTOCK CMF Plate, Titanium - Indonesia BPOM Medical Device Registration

REBSCTOCK CMF Plate, Titanium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420081. The device is manufactured by REBSTOCK INSTRUMENT GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BINA ARTHA SEMESTA.

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 : C
REBSCTOCK CMF Plate, Titanium
Analysis ID: AKL 21302420081

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

BINA ARTHA SEMESTA

AR Address

RUKO PERUMAHAN GREEN AREA KAV.C JL. GANDUL PLN

Registration Date

Mar 04, 2024

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Non Sterile

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