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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
HTL - STREFA S.A.Country of Origin
Poland
Authorized Representative
ANUGRAHMITRA IN LINEAR 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.
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