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MEDIQ Safety Lancet - PA - Indonesia BPOM Medical Device Registration

MEDIQ Safety Lancet - PA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422877. The device is manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOMAKMUR DWI LESTARI.

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
MEDIQ Safety Lancet - PA
Analysis ID: AKL 11603422877

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. INDOMAKMUR DWI LESTARI

AR Address

Ruko Mutiara taman palem blok A18 no 17 RT.7/RW.14, Cengkareng Tim., Kecamatan Cengkareng, Kota Jakarta Barat, Daerah Khusus Ibukota Jakarta 11730

Registration Date

Dec 16, 2024

Expiry Date

Dec 16, 2027

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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