JEOL Reagent Probe Wash 2 - Indonesia BPOM Medical Device Registration
JEOL Reagent Probe Wash 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420276. The device is manufactured by JEOL, LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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 : 1
Manufacturer
JEOL, LTD.Country of Origin
Japan
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Nov 11, 2024
Expiry Date
Aug 13, 2029
Product Type
Reagents and Specimen Providers
General purpose reagent.
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