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JOIMAX CESSYS Dorsal Cervical Posterior - Indonesia BPOM Medical Device Registration

JOIMAX CESSYS Dorsal Cervical Posterior is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21301220037. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
JOIMAX CESSYS Dorsal Cervical Posterior
Analysis ID: AKL 21301220037

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 19, 2023

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Orthopedic Equipment

Arthroscope

Non Radiation Electromedics

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