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MEDCARE Vacuum Regulator - Indonesia BPOM Medical Device Registration

MEDCARE Vacuum Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402220034. The device is manufactured by MEDCARE TECHNOLOGIES INC. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LUMARY BIRUMAS.

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
MEDCARE Vacuum Regulator
Analysis ID: AKL 10402220034

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. LUMARY BIRUMAS

AR Address

GEDUNG MENARA PALMA LT. 12, JL. HR RASUNA SAID BLOK X-2 KAV. 6

Registration Date

Jan 03, 2025

Expiry Date

Dec 30, 2027

Product Type

Monitoring Anesthesia Equipment

Pressure regulator.

Non Electromedic Non Sterile

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