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VICOM Sterile Syringe For Single Use - Indonesia BPOM Medical Device Registration

VICOM Sterile Syringe For Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902123869. The device is manufactured by SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIMARY WORKS.

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
VICOM Sterile Syringe For Single Use
Analysis ID: AKL 20902123869

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Jul 01, 2021

Expiry Date

Jul 01, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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