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ABBOTT m2000sp Instrument and Accessories (E-Series) - Indonesia BPOM Medical Device Registration

ABBOTT m2000sp Instrument and Accessories (E-Series) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102915552. The device is manufactured by TECAN SCHWEIZ AG. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN SYNERGY PROSPEROUS.

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 : A
ABBOTT m2000sp Instrument and Accessories (E-Series)
Analysis ID: AKL 10102915552

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

TECAN SCHWEIZ AG.

Country of Origin

Switzerland

Authorized Representative

PT. MAIN SYNERGY PROSPEROUS

AR Address

Gedung Menara Salemba Lt.3, Jl. Salemba Raya No.5-5A

Registration Date

Mar 04, 2024

Expiry Date

Dec 31, 2026

Product Type

Clinical Laboratory Equipment

General purpose laboratory equipment labeled or promoted for a specific medical use.

Invitro Diagnostics

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