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PHILIPS IntelliSite Pathology Solution - Indonesia BPOM Medical Device Registration

PHILIPS IntelliSite Pathology Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203026114. The device is manufactured by Philips Medical Systems Nederland B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHILIPS INDONESIA COMMERCIAL.

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
PHILIPS IntelliSite Pathology Solution
Analysis ID: AKL 20203026114

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Netherlands

Authorized Representative

PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005

Registration Date

Nov 04, 2024

Expiry Date

Jan 18, 2029

Product Type

Pathology Equipment and Accessories

Whole slide imaging system

Invitro Diagnostics

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