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CITOTEST Cryogenic Tube - Indonesia BPOM Medical Device Registration

CITOTEST Cryogenic Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203320298. The device is manufactured by CITOTEST LABWARE MANUFACTURING CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.

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
CITOTEST Cryogenic Tube
Analysis ID: AKL 10203320298

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ELO KARSA UTAMA

AR Address

Jl. Raya Kebayoran Lama No. 34E

Registration Date

Oct 04, 2023

Expiry Date

Jul 24, 2026

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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