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SUNMED Guide wires - Indonesia BPOM Medical Device Registration

SUNMED Guide wires is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501120599. The device is manufactured by SUNNY MEDICAL DEVICE (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GIRI SAKTI UTAMA.

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
SUNMED Guide wires
Analysis ID: AKL 20501120599

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GIRI SAKTI UTAMA

AR Address

Komp. Girimekar Permai Blok D No. 15 RT. 03 RW. 21 Desa Giri Mekar Kec. Cilengkrang

Registration Date

Feb 27, 2024

Expiry Date

Jan 16, 2027

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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