ThinPrep Genesis Processor - Indonesia BPOM Medical Device Registration
ThinPrep Genesis Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420112. The device is manufactured by HOLOGIC, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC 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 : 1
Manufacturer
HOLOGIC, INCCountry of Origin
United States
Authorized Representative
PT. BIOMEDIKAL SCIENTIFIC INDONESIAAR Address
18 Office Park 22nd F1 Suite E, F &G, Jalan TB SIMATUPANG 18
Registration Date
Jun 14, 2024
Expiry Date
Sep 30, 2025
Product Type
Pathology Equipment and Accessories
Tissue processing equipment
Invitro Diagnostics
Aptimaยฎ HIV-1 Quant Dx Assay
ThinPrep Pap Test Preservcyt Solution
ThinPrep Microscope Slides
ThinPrep Arcless Microscope Slides
ThinPrep Non-Gyn Filter
ThinPrep Gyn Filters
ThinPrep 2000 Processor and Accessories
APTIMA HBV Quant Assay Calibrator
ThinPrep 5000 Processor and Accessories
Thinprep PreservCyt Solution (NonGyn)
LIAISON XL Murex Control HBsAg
DIASORIN ITALIA S.P.A UK BRANCH
LIAISON XL Murex HBsAg
DIASORIN ITALIA S.P.A UK BRANCH
ThinPrep Pap Test Preservcyt Solution
HOLOGIC, INC
LIAISON Murex Anti-HEV IgM
Diasorin Italia S.p.A
LIAISON hGH
DIASORIN Italia S.P.A
LIAISON IGF-1
DIASORIN ITALIA S.P.A
LIAISON Murex Control Anti-HEV IgM
DIASORIN ITALIA S.P.A
LIAISON Murex Anti-HEV IgG
DIASORIN ITALIA S.P.A.
LIAISON Direct Renin
DIASORIN ITALIA S.P.A.
LIAISON Murex Control Anti-HEV IgG
DIASORIN ITALIA S.P.A.

