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SYNOLIS VA 40/80 - Indonesia BPOM Medical Device Registration

SYNOLIS VA 40/80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302122440. The device is manufactured by APTISSEN Ltd from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is I-TECH LAFACOS.

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BPOM Registered
Risk Class Kelas Resiko : D
SYNOLIS VA 40/80
Analysis ID: AKL 31302122440

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

APTISSEN Ltd

Country of Origin

Switzerland

Authorized Representative

I-TECH LAFACOS

AR Address

Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih

Registration Date

May 17, 2021

Expiry Date

Jun 25, 2025

Product Type

Prosthetic Orthopedic Equipment

Intra articular fluid

Non Electromedic Sterile

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