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ZENER GENERAL SPINAL SYSTEM - Indonesia BPOM Medical Device Registration

ZENER GENERAL SPINAL SYSTEM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321017. The device is manufactured by ZENER MEDTEC (CHANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ADHIRA MEDIKA PERSADA INTERNATIONAL.

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
ZENER GENERAL SPINAL SYSTEM
Analysis ID: AKL 21302321017

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

AR Address

Ruko Paramount Sparks B No. 17, Jl. Raya Kelapa Dua Gading Serpong

Registration Date

Nov 28, 2023

Expiry Date

Aug 08, 2027

Product Type

Prosthetic Orthopedic Equipment

Spinal interlaminal fixation orthosis.

Non Electromedic Non Sterile

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