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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
DISTIMP SASCountry of Origin
France
Authorized Representative
ORIONTAMA JAYAAR 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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