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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
Philips Medical Systems Nederland B.V.Country of Origin
Netherlands
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR 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
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