DEFINISSE™ - Indonesia BPOM Medical Device Registration
DEFINISSE™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324513. The device is manufactured by ASSUT EUROPE S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSFARMA MEDICA INDAH.
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
ASSUT EUROPE S.P.ACountry of Origin
Italy
Authorized Representative
PT. TRANSFARMA MEDICA INDAHAR Address
Unit 802, 8th Fl. Wisma Pondok Indah 2, Jl. Sultan Iskandar Muda Kav V-TA, Pondok Indah
Registration Date
Jun 18, 2024
Expiry Date
May 04, 2027
Product Type
Surgical Equipment
Absorbable poly(glycolide/ l -lactide) surgical suture.
Non Electromedic Sterile
ABBOCATH-T
AMSINO MEDICAL (SHANGHAI) CO., LTD.
QUIXX ™ Sore Throat Spray Kids
VITROBIO SAS
QUIXX ™ Sore Throat Spray
VITROBIO SAS
ATOPICLAIR Cream
BIOKOSMES S.R.L.
DEFINISSE Hydrobooster
CROMA-PHARMA GMBH
DEFINE Core Filler + Lidocaine
CROMA-PHARMA GMBH
DEFINISSE Restore Filler + Lidocaine
CROMA-PHARMA GMBH
DEFINE Touch Filler + Lidocaine
CROMA-PHARMA GMBH
RELIZEMA cream
BIOKOSMES S.R.L
ATOPICLAIR Lotion
BIOKOSMES S.R.L.

