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NESCO Lanze Lancing Device - Indonesia BPOM Medical Device Registration

NESCO Lanze Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603325893. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
NESCO Lanze Lancing Device
Analysis ID: AKL 11603325893

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

Dec 27, 2023

Expiry Date

Dec 26, 2026

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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