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SYMBIOZ CAM - Indonesia BPOM Medical Device Registration

SYMBIOZ CAM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801710999. The device is manufactured by PUFF. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. VERSACON MEDICAL.

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 : B
SYMBIOZ CAM
Analysis ID: AKL 20801710999

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PUFF.

Country of Origin

France

Authorized Representative

PT. VERSACON MEDICAL

AR Address

JL ANGGREK NELI MURNI BLOK C NO 30-30 A, PALMERAH

Registration Date

Apr 17, 2020

Expiry Date

Mar 25, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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