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HAEMOLANCE Plus Safety Lancets - Indonesia BPOM Medical Device Registration

HAEMOLANCE Plus Safety Lancets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603512454. The device is manufactured by HTL - STREFA S.A. from Poland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ANUGRAHMITRA IN LINE.

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
HAEMOLANCE Plus Safety Lancets
Analysis ID: AKL 11603512454

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

HTL - STREFA S.A.

Country of Origin

Poland

Authorized Representative

ANUGRAHMITRA IN LINE

AR Address

Jl. Agung Niaga IV Blok G.4 No. 54 Kel. Sunter Agung, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Jun 16, 2023

Expiry Date

Mar 31, 2026

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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