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GBLAB Sample Cup - Indonesia BPOM Medical Device Registration

GBLAB Sample Cup is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203814511. The device is manufactured by NINGBO FOYOMED MEDICAL INSTRUMENTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BERLIANTAMA DIAGNOSTIKA 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
GBLAB Sample Cup
Analysis ID: AKL 10203814511

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

BERLIANTAMA DIAGNOSTIKA INDONESIA

AR Address

JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16

Registration Date

Jul 15, 2021

Expiry Date

Jun 01, 2024

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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