Device classification

Heparin, Vascular Access Flush

General Hospital · 21 CFR 880.5200

Class IIProduct code NZW
Open FDA's page for this record
Third party flag
N
Life sustain support flag
N
Gmp exempt flag
N
Summary malfunction reporting
Eligible
Product code
NZW
Review panel
HO
Medical specialty
HO
Device name
Heparin, Vascular Access Flush
Medical specialty description
General Hospital
Device class
2
Definition
Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.
Regulation number
880.5200
Implant flag
N
Submission type ID
1
Harmonized identifiers (openFDA)
K number
K061497, K092491, K133446, K090680, K092938, K023740, K163591
Registration number
1423507, 3011689956, 2243072, 3012421607, 3008518459, 2027791, 1423982, 1911916
FEI number
3011689956, 2243072, 3001677091, 3012421607, 3008518459, 1000122362, 1911916, 3008002452
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.