BOECO CENTRIFUGE M-240 - Indonesia BPOM Medical Device Registration
BOECO CENTRIFUGE M-240 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205024406. The device is manufactured by ANDREAS HETTICH GMBH + CO. KG, GERMANY from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BAVARIA COMBININDO.
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
ANDREAS HETTICH GMBH + CO. KG, GERMANYCountry of Origin
Germany
Authorized Representative
PT. BAVARIA COMBININDOAR Address
JL. CILEDUG RAYA NO. 232 KEBAYORAN LAMA
Registration Date
Jul 14, 2021
Expiry Date
Jan 21, 2026
Product Type
Automatic and Semi-Automatic Hematology Equipment
Microsedimentation centrifuge.
Invitro Diagnostics
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MTD DIAGNOSTICS SRL.
MTD Chemistry Control N
MTD DIAGNOSTICS SRL.
HDL DIRECT LS
MTD DIAGNOSTICS SRL.
MTD gGT Sz74 LS 4+1
MTD DIAGNOSTICS SRL.
MTD DIAGNOSTICS BILIRUBIN T LS 2nd GEN 4+1
MTD DIAGNOSTICS SRL.
CHEMISTRY MULTICALIBRATOR
MTD DIAGNOSTICS SRL.
MTD TRIGLYCERIDES GPO-PAP LS Mono
MTD DIAGNOSTICS SRL.
MTD GOT ASAT IFCC LS 4+1
MTD DIAGNOSTICS SRL.
MTD Uric Acid Uricase PAP LS Mono
MTD DIAGNOSTICS SRL.
MTD GLUCOSE GOD-PAP LS Mono
MTD DIAGNOSTICS SRL.

