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NODFORD Microcentrifuge Tube - Indonesia BPOM Medical Device Registration

NODFORD Microcentrifuge Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203121140. The device is manufactured by SHENZHEN NODFORD INDUSTRIAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
NODFORD Microcentrifuge Tube
Analysis ID: AKL 10203121140

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SABA INDOMEDIKA

AR Address

KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN

Registration Date

Mar 03, 2021

Expiry Date

Dec 17, 2023

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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