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NESCO Lancing Device - Indonesia BPOM Medical Device Registration

NESCO Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603022063. The device is manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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 : A
NESCO Lancing Device
Analysis ID: AKL 11603022063

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420

Registration Date

May 04, 2023

Expiry Date

May 01, 2026

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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