T-Cell Xtend - Indonesia BPOM Medical Device Registration
T-Cell Xtend is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303124736. The device is manufactured by OXFORD IMMUNOTEC LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OXFORD IMUNOTEK 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 : 2
Manufacturer
OXFORD IMMUNOTEC LTDCountry of Origin
United Kingdom
Authorized Representative
PT. OXFORD IMUNOTEK INDONESIAAR Address
Mixed Home Savoy B1-36, Jalan Perumahan Jakarta Garden City Boulevard RT 001 RW 006
Registration Date
Aug 02, 2021
Expiry Date
Mar 01, 2026
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
Invitro Diagnostics
Auto-Pure 2400 and Accessories Automatic Cell Separation System
HANGZHOU ALLSHENG INSTRUMENTS CO.,LTD
AIM-V Medium
LIFE TECHNOLOGIES CORPORATION
LEUCOSEP TUBES
GREINER BIO-ONE
ALLSHENG Nucleic Acid Purification System Auto-Pure24
HANGZHOU ALLSHENG INSTRUMENTS CO.,LTD
T-Cell Select
OXFORD IMMUNOTEC LTD
T-SPOT. TB
OXFORD IMMUNOTEC LIMITED

