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KIFAMED Sterile Hypodermic Syringe for Single Use - Indonesia BPOM Medical Device Registration

KIFAMED Sterile Hypodermic Syringe for Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220039. The device is manufactured by HUNAN PINGAN MEDICAL DEVICE TECHNOLOGY, CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIMIA FARMA TBK..

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
KIFAMED Sterile Hypodermic Syringe for Single Use
Analysis ID: AKL 20902220039

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KIMIA FARMA TBK.

AR Address

Jalan Veteran No.9

Registration Date

Jan 17, 2022

Expiry Date

Jan 17, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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