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LEUCOSEP TUBES - Indonesia BPOM Medical Device Registration

LEUCOSEP TUBES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203320245. The device is manufactured by GREINER BIO-ONE from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OXFORD IMUNOTEK 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 : A
LEUCOSEP TUBES
Analysis ID: AKL 10203320245

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

GREINER BIO-ONE

Country of Origin

Germany

Authorized Representative

PT. OXFORD IMUNOTEK INDONESIA

AR Address

Mixed Home Savoy B1-36, Jalan Perumahan Jakarta Garden City Boulevard RT 001 RW 006

Registration Date

Jul 17, 2023

Expiry Date

Nov 01, 2027

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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