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NESCO Lancets - Indonesia BPOM Medical Device Registration

NESCO Lancets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603811348. The device is manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCT 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 Lancets
Analysis ID: AKL 11603811348

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

Registration Date

Feb 26, 2021

Expiry Date

Dec 31, 2023

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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