ZELTIQ CoolSculpting System Accessories - Indonesia BPOM Medical Device Registration
ZELTIQ CoolSculpting System Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603021154. The device is manufactured by ZELTIQ IRELAND UNLIMITED COMPANY from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHARMINDO LESTARI AWARD.
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
ZELTIQ IRELAND UNLIMITED COMPANYCountry of Origin
Ireland
Authorized Representative
PT. PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta
Registration Date
Mar 17, 2020
Expiry Date
Nov 26, 2024
Product Type
Surgical Equipment
Contact cooling system for aesthetic use
Non Radiation Electromedics
GC Tooth Mousse Milkshake
GC CORPORATION FUJI OYAMA FACTORY
PROFHILO STRUCTURA 4.5%
IBSA FARMACEUTICI ITALIA SRL
G-AENIAL Universal Flo
GC DENTAL PRODUCTS CORPORATION
JUVEDERM Volbella with Lidocaine
ALLERGAN
JUVEDERM Ultra Plus XC
ALLERGAN
JUVEDERM VOLUX
ALLERGAN
JUVEDERM VOLIFT with Lidocaine
ALLERGAN
JUVEDERM VOLUMA with Lidocaine
ALLERGAN
JUVEDERM Likes
ALLERGAN
HYAL SYSTEM 1.8%
FIDIA FARMACEUTICI S.P.A.