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ANTMED High Pressure Syringe - Indonesia BPOM Medical Device Registration

ANTMED High Pressure Syringe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501026369. The device is manufactured by SHENZHEN ANTMED CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DERMARELIS.

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 : C
ANTMED High Pressure Syringe
Analysis ID: AKL 20501026369

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DERMARELIS

AR Address

Gedung Pembina Graha Blok 2 Ruang 214, Jl. DI Panjaitan 45, RT.017. RW.006, Kel. Rawa Bunga.

Registration Date

Aug 20, 2024

Expiry Date

Aug 27, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Electromedic Sterile

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