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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.

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BPOM Registered
Risk Class Kelas Resiko : B
SWELAB Alfa Plus Standard and Accessories
Analysis ID: AKL 20205320299

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BOULE MEDICAL, AB

Country of Origin

Sweden

Authorized Representative

PT. SWELAB INDONESIA

AR 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

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