CAVEX – Silicon A Heavy Body - Indonesia BPOM Medical Device Registration
CAVEX – Silicon A Heavy Body is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602816924. The device is manufactured by CAVEX HOLLAND B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.
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
CAVEX HOLLAND B.V.Country of Origin
Netherlands
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47
Registration Date
Sep 03, 2021
Expiry Date
Dec 31, 2024
Product Type
Prosthetic Dental Equipment
Impression material.
Non Electromedic Non Sterile
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