TRILOGY EV300 - Indonesia BPOM Medical Device Registration
TRILOGY EV300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403023146. The device is manufactured by RESPIRONICS INC. from United States, and is classified as Risk Class Kelas Resiko : C. 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
RESPIRONICS INC.Country of Origin
United States
Authorized Representative
PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005
Registration Date
Jan 02, 2025
Expiry Date
Oct 30, 2029
Product Type
Therapeutic Anesthesia Equipment
Continuous ventilator.
Non Radiation Electromedics
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TRILOGY EVO
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PHILIPS CT 5300
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PHILIPS CT 5300
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PHILIPS CT 5300
PHILIPS HEALTHCARE (SUZHOU) CO., LTD.
EPIQ 5 Diagnostic Ultrasound System
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