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ONEMED Dry Bath - Indonesia BPOM Medical Device Registration

ONEMED Dry Bath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220023. The device is manufactured by DLAB SCIENTIFIC CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INTIGLOBAL PERFECT RESULT SOURCE.

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 : B
ONEMED Dry Bath
Analysis ID: AKL 20209220023

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Feb 23, 2022

Expiry Date

Feb 23, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Blood and plasma warming device.

Invitro Diagnostics

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DJ Fang

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