FDA Registration Active 🇩🇰 Denmark

RADIOMETER MEDICAL APS

Reg #: 3002807968 · FEI: 3002807968 · Expires 2026
Products
26
Proprietary Names
4
Establishment Types
2
Classifications
26

Registration Details

Registration Name
RADIOMETER MEDICAL APS
Registration Number
3002807968
FEI Number
3002807968
Status
Active
Expiry Year
2026
Initial Importer
No
Address
AAKANDEVEJ 21
City
BROENSHOEJ Hovedstaden
Country
DK

Regulatory Submissions

510(k) Number
K092686

Owner / Operator

Firm Name
Radiometer Medical ApS
Operator Number
9064213
Address
AAKANDEVEJ 21, --
City
BROENSHOEJ
State
Hovedstaden
Postal Code
2700
Country
DK
Correspondent
Hsiao-Qing Chow

US Agent

Business Name
RADIOMETER AMERICA, INC.
Contact Name
MATT ACKERMAN
Address
250 S Kraemer Blvd
City
Brea
State
CA
ZIP
92821
Country
US
Phone
657 2861022

Products

Device Name Product Code
Medical Device Data System OUG
Electrode, Ion Specific, Calcium JFP
Electrode, Ion Specific, Sodium JGS
Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph CHL
Assay, Fetal Hemoglobin KQI
Multi-Analyte Controls, All Kinds (Assayed) JJY
Acid, Lactic, Enzymatic Method KHP
Calibrator, Multi-Analyte Mixture JIX
System, Hemoglobin, Automated GKR
Glucose Oxidase, Glucose CGA
Electrode, Ion Specific, Potassium CEM
Electrode, Ion-Specific, Chloride CGZ
Assay, Carboxyhemoglobin GHS
Tubes, Vials, Systems, Serum Separators, Blood Collection JKA
Syringe, Antistick MEG
Oximeter, Ear DPZ
Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia KLK
Monitor, Carbon-Dioxide, Cutaneous LKD
Oximeter DQA
Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia LPP
Controls For Blood-Gases, (Assayed And Unassayed) JJS
Electrode, Ion Based, Enzymatic, Creatinine CGL
Bilirubin (Total And Unbound) In The Neonate Test System MQM
Instrument, Hematocrit, Automated GKF
Diazo Colorimetry, Bilirubin CIG
Tube, Collection, Capillary Blood GIO

Proprietary Names

ABL90 FLEX PLUS TCM400 Monitoring System 956-533 PICO70 23Gx25 mm ABL90 FLEX

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device