BEHNK Thrombolyzer XR Coagulation Analyzer - Indonesia BPOM Medical Device Registration
BEHNK Thrombolyzer XR Coagulation Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205510484. The device is manufactured by KOMMANDITGESELLSCHRAFT BEHNK ELEKTRONIK GMBH & CO. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTI SARANA MEDIKA.
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
Country of Origin
Germany
Authorized Representative
PT. MULTI SARANA MEDIKAAR Address
Komp. Gading Bukit Indah Jl. Bukit Gading Raya Blok B Kav. No.1
Registration Date
Feb 27, 2024
Expiry Date
Sep 11, 2026
Product Type
Automatic and Semi-Automatic Hematology Equipment
Coagulation instrument.
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