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MEDI Spinomed IV - Indonesia BPOM Medical Device Registration

MEDI Spinomed IV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402915329. The device is manufactured by MEDI GMBH. & CO., KG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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 : A
MEDI Spinomed IV
Analysis ID: AKL 11402915329

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Nov 05, 2019

Expiry Date

Sep 05, 2024

Product Type

Prosthetic Physical Health Equipment

Truncal orthosis.

Non Electromedic Non Sterile

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