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ONEMED Spacer for Aerosol - Indonesia BPOM Medical Device Registration

ONEMED Spacer for Aerosol is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420499. The device is manufactured by TAIAN DALU MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 Spacer for Aerosol
Analysis ID: AKL 20403420499

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INTIGLOBAL PERFECT RESULT SOURCE

AR Address

KOMPLEK DARMO PARK II BLOK 4/14

Registration Date

Jul 08, 2024

Expiry Date

Jul 07, 2027

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Electromedic Non Sterile

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