DRAEGER Jaundice Meter - Indonesia BPOM Medical Device Registration
DRAEGER Jaundice Meter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101511942. The device is manufactured by DRAEGER MEDICAL SYSTEM INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DRAEGER MEDICAL 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
DRAEGER MEDICAL SYSTEM INC.Country of Origin
United States
Authorized Representative
PT. DRAEGER MEDICAL INDONESIAAR Address
ALAMANDA TOWER Lt. 32 Unit A,B,D,E,F. Jl. TB. Simatupang Kav. 23-24
Registration Date
Dec 21, 2023
Expiry Date
Apr 18, 2027
Product Type
Clinical Chemistry Test System
Bilirubin (total and unbound) in the neonate test system
Non Radiation Electromedics
DRAEGER Mobile Patient Watch
DRAEGERWERK AG & CO. KGAA.
DRAEGER Alcotest 7000
DRAEGER SAFETY AT & CO. KGAA
INFINITY M300 Patient Monitor
DRAEGER MEDICAL SYSTEMS, INC.
DRAEGER INFINITY Central Station
DRAEGER MEDICAL SYSTEMS, INC.
Draeger ATLAN A100
DRAEGERWERK AG. & CO. KGAA.
DRAEGER ATLAN A100 XL
DRAEGERWERK AG. & CO. KGAA.
ATLAN A300 XL Anesthesia Machine
DRAEGERWERK AG & CO. KGAA
ATLAN A350 XL Anesthesia Machine
DRAEGERWERK AG. & CO. KGAA.
ATLAN A300 Anesthesia Machine
DRAEGERWERK AG & CO. KGAA
DRAEGER Resuscitaire
DRAEGER MEDICAL SYSTEMS INC.

