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PENTAX MEDICAL USB CAMERA KIT - Indonesia BPOM Medical Device Registration

PENTAX MEDICAL USB CAMERA KIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801020063. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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
PENTAX MEDICAL USB CAMERA KIT
Analysis ID: AKL 20801020063

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PUFF

Country of Origin

France

Authorized Representative

PT. PRO-HEALTH INTERNATIONAL

AR Address

Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5

Registration Date

Nov 09, 2022

Expiry Date

Oct 31, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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