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CASPAR Evolution System - Indonesia BPOM Medical Device Registration

CASPAR Evolution System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302905588. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
CASPAR Evolution System
Analysis ID: AKL 21302905588

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

AESCULAP AG

Country of Origin

Germany

Authorized Representative

B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Sep 19, 2024

Expiry Date

Mar 01, 2027

Product Type

Prosthetic Orthopedic Equipment

Spinal interlaminal fixation orthosis.

Non Electromedic Sterile

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