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VITRA 2 - Indonesia BPOM Medical Device Registration

VITRA 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203915129. The device is manufactured by QUANTEL MEDICAL from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SURYA TAMA MEDIKA.

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 : C
VITRA 2
Analysis ID: AKL 21203915129

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

QUANTEL MEDICAL

Country of Origin

France

Authorized Representative

SURYA TAMA MEDIKA

AR Address

Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi

Registration Date

Jan 23, 2024

Expiry Date

Jan 17, 2029

Product Type

Surgical Eye Equipment

Ophthalmic photocoagulator.

Non Radiation Electromedics

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