Vietnam MOH registration 240002354/PCBA-HN
IVD is the dilution solution for the sample
VN: IVD là dung dịch pha loãng mẫu
Registration details
- Analysis ID
- 240002354/PCBA-HN
- Submission ID
- 000.00.19.H26-241023-0014
- Product Type
- Lumipulse G Specimen Diluent 4
Company information
- Manufacturer
- Fujirebio Inc. Sagamihara Facility
- Manufacturer Country
- JAPAN
- Product Owner
- Fujirebio Inc.
- Authorized Representative
- CÔNG TY TNHH ARQON VIỆT NAM
Technical details
- Intended Use
- For in vitro diagnosis only: This product is a special reagent to dilute samples in Lumipulse G T3 and T4. This product is intended for professional use only.
Dates and status
- Registration Date
- Oct 24, 2024
About this record
Access comprehensive regulatory information for IVD is the dilution solution for the sample in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TBYT Loại A medical device is registered under number 240002354/PCBA-HN and manufactured by Fujirebio Inc. Sagamihara Facility. The authorized representative in Vietnam is CÔNG TY TNHH ARQON VIỆT NAM.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI300,000+ Devices