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SMARTCARE-Tourniquet - Indonesia BPOM Medical Device Registration

SMARTCARE-Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604320042. The device is manufactured by SHENZHEN TMI MEDICAL SUPPLIES CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SMART CARE 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
SMARTCARE-Tourniquet
Analysis ID: AKL 11604320042

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SMART CARE INDONESIA

AR Address

VILLA(RUKO ) MELATI MAS SQUARE BLOK A.3 NO. 8, JELUPANG, SERPONG UTARA,TANGERANG SELATAN

Registration Date

Oct 20, 2023

Expiry Date

Oct 19, 2026

Product Type

Therapeutic Surgical Equipment

Nonpneumatic tourniquet.

Non Electromedic Non Sterile

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