VIDELAB Plain Tube No Additive - Indonesia BPOM Medical Device Registration
VIDELAB Plain Tube No Additive is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101027196. The device is manufactured by HEBEI XINLE SCI & TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SARANA MAJU SEJAHTERA.
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
HEBEI XINLE SCI & TECH CO., LTD.Country of Origin
China
Authorized Representative
SARANA MAJU SEJAHTERAAR Address
Jl. Johar No.2, Kebon Sirih, Menteng,
Registration Date
Feb 06, 2022
Expiry Date
Feb 05, 2025
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
GB Lab Vacuum Tube Plain Glass
GB Lab Vacuum Tube SST Gel
GB Lab Vacuum Tube Serum Clot Activator
GB Lab Vacuum Tube EDTA K3 GLASS
VIDELAB Gel & Clot Activator Tube GLASS
VIDELAB Pro-Coagulation Tube Clot Activator PET
VIDELAB Plain Tube No Additive
Labnovation Hemoglobin A1c Test Kit (Boronate Affinity)
LABNOVATION TECHNOLOGIES, INC.,
Labnovation Lyser HGB
LABNOVATION TECHNOLOGIES, INC.,
Labnovation Diluent M
LABNOVATION TECHNOLOGIES, INC.,
URINA-120 Urine Analyzer
URIT MEDICAL ELECTRONIC CO., LTD
URIT CA-80 Semi-Automatic Chemistry Analyzer
URIT MEDICAL ELECTRONIC CO., LTD
LABNOVATION Cleanac NK
LABNOVATION TECHNOLOGIES INC.

