ARCHITECT Pre-Trigger Solution - Indonesia BPOM Medical Device Registration
ARCHITECT Pre-Trigger Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20204418091. The device is manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ABBOTT IRELAND DIAGNOSTICS DIVISION.Country of Origin
Ireland
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA
Registration Date
May 22, 2019
Expiry Date
Mar 12, 2024
Product Type
Reagents and Specimen Providers
Analyte specific reagents.
Invitro Diagnostics
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MITRACLIP G4 Steerable Guide Catheter
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