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CELLAVISION DC-1 and Accessories - Indonesia BPOM Medical Device Registration

CELLAVISION DC-1 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205026203. The device is manufactured by CELLAVISION AB. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SABA INDOMEDIKA.

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
CELLAVISION DC-1 and Accessories
Analysis ID: AKL 20205026203

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CELLAVISION AB.

Country of Origin

Sweden

Authorized Representative

PT. SABA INDOMEDIKA

AR Address

KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN

Registration Date

Oct 16, 2020

Expiry Date

Aug 17, 2025

Product Type

Automatic and Semi-Automatic Hematology Equipment

Automated cell-locating device.

Invitro Diagnostics

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