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Proteor Dynastar ( Foot Foot ) - Indonesia BPOM Medical Device Registration

Proteor Dynastar ( Foot Foot ) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402220176. The device is manufactured by PROTEOR from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ORTHOCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
Proteor Dynastar ( Foot Foot )

Proteor Dynastar ( Pied Foot )

Analysis ID: AKL 11402220176

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

PROTEOR

Country of Origin

France

Authorized Representative

PT. ORTHOCARE INDONESIA

AR Address

RUKO GALERI NIAGA MEDITERNIA 2 BLOK N 8 J , JL.PANTAI INDAH UTARA II RT/RW : 007/008 KEL KAPUK MUARA KEC. PENJARINGAN KOTA ADM JAKARTA UTARA

Registration Date

Jul 11, 2022

Expiry Date

Jan 31, 2027

Product Type

Prosthetic Physical Health Equipment

Prosthetic and orthotic accessory.

Non Electromedic Non Sterile

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