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JOIMAX Shrill Spine Pump - Indonesia BPOM Medical Device Registration

JOIMAX Shrill Spine Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303411279. The device is manufactured by JOIMAX GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTEK.

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 : B
JOIMAX Shrill Spine Pump
Analysis ID: AKL 21303411279

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

JOIMAX GMBH.

Country of Origin

Germany

Authorized Representative

PT. MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Jun 29, 2020

Expiry Date

Dec 31, 2023

Product Type

Surgical Orthopaedic Equipment

Sonic surgical instrument and accessories/attachments.

Non Radiation Electromedics

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