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ANGIO-SEAL VIP Vascular Closure Device - Indonesia BPOM Medical Device Registration

ANGIO-SEAL VIP Vascular Closure Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505810971. The device is manufactured by TERUMO PUERTO RICO LLC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TERUMO 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 : D
ANGIO-SEAL VIP Vascular Closure Device
Analysis ID: AKL 30505810971

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Oct 31, 2023

Expiry Date

Sep 22, 2028

Product Type

Therapeutic Cardiology Equipment

Vascular Hemostatis Device

Non Electromedic Sterile

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