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PD NGT Silicone Tube - Indonesia BPOM Medical Device Registration

PD NGT Silicone Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220448. The device is manufactured by HITEC MEDICAL CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BETWEEN PARTNERS OF SELF-SUFFICIENCY.

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
PD NGT Silicone Tube
Analysis ID: AKL 20805220448

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

AR Address

Jl. Pos Pengumben Raya No.8 RT.005 RW.005, Sukabumi Selatan, Kebon Jeruk, Jakarta Barat 11560

Registration Date

Nov 23, 2022

Expiry Date

Aug 08, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Gastrointestinal tube and accessories.

Non Electromedic Sterile

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