SWELAB Alfa Plus Standard and Accessories - Indonesia BPOM Medical Device Registration
SWELAB Alfa Plus Standard and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205320299. The device is manufactured by BOULE MEDICAL, AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SWELAB 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
BOULE MEDICAL, ABCountry of Origin
Sweden
Authorized Representative
PT. SWELAB INDONESIAAR Address
HBR Motik Komplek Taman Kumala Burlian Blok R/14
Registration Date
Mar 13, 2024
Expiry Date
Feb 07, 2026
Product Type
Automatic and Semi-Automatic Hematology Equipment
Automated cell counter.
Invitro Diagnostics
BOULE Con-Diff N
BOULE MEDICAL, AB
BOULE Con-Diff Tri L
BOULE MEDICAL, AB
BALL Cal
BOULE MEDICAL, AB
BOULE Con-5Diff A1 Norm
BOULE MEDICAL.
BALL Cal-5Diff A1
BOULE MEDICAL.
BALL Con-5Diff A1 Tri
BOULE MEDICAL AB
ECG - Expert
CUSTOM SOFTWARE & ELECTRONICS, S.L.
QUINTUS 5-part Hematology Analyzer and Accessories
BOULE MEDICAL.
SWELAB Alfa Plus Cap and Accessories
BOULE MEDICAL.
SWELAB ALFA Plus Sampler
BOULE MEDICAL.

