FDA Registration Active 🇺🇸 United States

RAPIDPoint® 500e Blood Gas System

Reg #: 3002637618 · FEI: 3002637618 · Expires 2025
Products
9
Proprietary Names
2
Establishment Types
2
Classifications
9

Registration Details

Registration Name
Siemens Healthcare Diagnostics Inc
Registration Number
3002637618
FEI Number
3002637618
Status
Active
Expiry Year
2025
Initial Importer
No
Address
Point Of Care Headquarters, 333 Coney St
City
East Walpole
State
MA
ZIP
02032
Country
US

Regulatory Submissions

510(k) Number
K192240

Owner / Operator

Firm Name
SIEMENS HEALTHCARE DIAGNOSTICS INC.
Operator Number
9096044
Address
Siemens Healthcare Diagnostics Inc., 511 Benedict Avenue
City
Tarrytown
State
NY
Postal Code
10591
Country
US

Products

Device Name Product Code
Electrode, Ion Specific, Sodium JGS
Electrode, Ion-Specific, Chloride CGZ
Electrode, Ion Specific, Potassium CEM
Acid, Lactic, Enzymatic Method KHP
Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph CHL
Electrode, Ion Specific, Calcium JFP
Glucose Oxidase, Glucose CGA
Bilirubin (Total And Unbound) In The Neonate Test System MQM
System, Hemoglobin, Automated GKR

Proprietary Names

RAPIDPoint® 500e Blood Gas System iCa++ Quick Sampler

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility