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ACIFBOX Spine Implants - Indonesia BPOM Medical Device Registration

ACIFBOX Spine Implants is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320588. The device is manufactured by DISTIMP SAS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ORIONTAMA JAYA.

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
ACIFBOX Spine Implants
Analysis ID: AKL 21302320588

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

DISTIMP SAS

Country of Origin

France

Authorized Representative

ORIONTAMA JAYA

AR Address

Jl. Sutomo No. 122-124, Medan

Registration Date

Mar 15, 2023

Expiry Date

Nov 02, 2027

Product Type

Prosthetic Orthopedic Equipment

Intervertebral body fusion device

Non Electromedic Non Sterile

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