KAPHORN Spine Implants - Indonesia BPOM Medical Device Registration
KAPHORN Spine Implants is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420012. 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
Jan 16, 2024
Expiry Date
Nov 02, 2027
Product Type
Prosthetic Orthopedic Equipment
Pedicle screw spinal system
Non Electromedic Non Sterile
MJBIO Drain Canister
GUANGDONG MEIJI BIOTECHNOLOGY CO., LTD.
LP-ESP Disc Prosthesis
SPINE INNOVATIONS
MJBIO Medical Negative Pressure Suction Device
GUANGDONG MEIJI BIOTECHNOLOGY CO., LTD.
MJBIO Vacuum Sealed Irrigation Wound Therapy Kit
GUANGDONG MEIJI BIOTECHNOLOGY CO., LTD.
KAPHORN Surgical Intruments
DISTIMP SAS
VEOS Spine Implants
DISTIMP SAS
ABLE Disposable Abdomen Drainage Catheters
GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD
ACIFBOX Surgical Instruments
DISTIMP SAS
ACIFBOX Spine Implants
DISTIMP SAS
MG Disposable Hemoperfusion Cartridge
FOSHAN BIOSUN MEDICAL TECHNOLOGY CO., LTD

