BD Ultra-Fine ™ PRO - Indonesia BPOM Medical Device Registration
BD Ultra-Fine ™ PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902911308. The device is manufactured by BECTON DICKINSON AND COMPANY from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BECTON DICKINSON INDONESIA.
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 : 2
Manufacturer
BECTON DICKINSON AND COMPANYCountry of Origin
Ireland
Authorized Representative
BECTON DICKINSON INDONESIAAR Address
SAMPOERNA STRATEGIC SQUARE, SOUTH TOWER LT.20 JL. JEND SUDIRMAN KAV 45-46
Registration Date
Aug 15, 2023
Expiry Date
Nov 29, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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