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JBP Nano Cannula - Indonesia BPOM Medical Device Registration

JBP Nano Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902121503. The device is manufactured by FEEL-TECH CO, LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REGENESIS 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 : B
JBP Nano Cannula
Analysis ID: AKL 20902121503

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

FEEL-TECH CO, LTD

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan

Registration Date

Mar 18, 2021

Expiry Date

Nov 24, 2023

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

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