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VACUSERA Automatic Tourniquet - Indonesia BPOM Medical Device Registration

VACUSERA Automatic Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504912259. The device is manufactured by DISERA MEDICAL MATERIAL LOGISTICS INDUSTRY AND TRADE JOINT STOCK COMPANY. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HOSPI MEDIK 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 : B
VACUSERA Automatic Tourniquet
Analysis ID: AKL 20504912259

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. HOSPI MEDIK INDONESIA

AR Address

Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520

Registration Date

Sep 26, 2024

Expiry Date

Dec 31, 2026

Product Type

Surgical Cardiology Equipment

Vascular clamp.

Non Electromedic Non Sterile

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