SELLA Lancing Device - Indonesia BPOM Medical Device Registration
SELLA Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603717064. The device is manufactured by HOSPITAL AND HOMECARE IMP. & EXP. CO. LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA AGUNG MANDIRI.
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
HOSPITAL AND HOMECARE IMP. & EXP. CO. LTD.Country of Origin
China
Authorized Representative
PT. DAYA AGUNG MANDIRIAR Address
JL S. HASANUDIN NO 23 PERUM POLEKO RT 001/001 DESA TAMBUN KEC TAMBUN SELATAN
Registration Date
Jan 13, 2022
Expiry Date
May 13, 2025
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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