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POLYMED Huber Infusion Set - Indonesia BPOM Medical Device Registration

POLYMED Huber Infusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322813. The device is manufactured by POLY MEDICURE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.

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
POLYMED Huber Infusion Set
Analysis ID: AKL 20902322813

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. BISAWI GROWS IN HARMONY

AR Address

Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat

Registration Date

Aug 26, 2024

Expiry Date

Feb 15, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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