BD MAX™ MDR-TB - Indonesia BPOM Medical Device Registration
BD MAX™ MDR-TB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302128062. The device is manufactured by GENEOHM SCIENCES CANADA INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BECTON DICKINSON 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 : 2
Manufacturer
GENEOHM SCIENCES CANADA INC.Country of Origin
Canada
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
SAMPOERNA STRATEGIC SQUARE, SOUTH TOWER LT.20 JL. JEND SUDIRMAN KAV 45-46
Registration Date
Nov 23, 2023
Expiry Date
Jan 05, 2025
Product Type
Microbiology Equipment
Microorganism differentiation and identification device.
Invitro Diagnostics
BD Gravity IV Set with ARD Technology and AutoPrime
CAREFUSION BH 335 D.O.O CAZIN
AST-Reagent Kit
MERLIN DIAGNOSTIKA GMBH
BD BBL™ Sensi-Disc™ CEFTRIAXONE 30 µg
BECTON DICKINSON CARIBE LTD.
BD Leucocount™ Kit
BECTON DICKINSON CARIBE, LTD.
BD BBL™ Sensi-Disc™ Levofloxacin 5 µg
BECTON DICKINSON CARIBE LTD.
BD Onclarity™ HPV Assay Reagent Pack
BECTON, DICKINSON AND COMPANY
BD BBL Sensi-Disc Colistin 10 µg
BECTON DICKINSON CARIBE LTD.
BD FC Beads 7-Color Kit
BECTON DICKINSON CARIBE, LTD.
BD POSIFLUSH SP Syringe
BECTON DICKINSON, S.A.
BD BBL™ Sensi-Disc™ CHLORAMPHENICOL 30 µg
BECTON DICKINSON CARIBE LTD.