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U.S. Department of Health and Human Services

Establishment Registration & Device Listing
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Proprietary Name: (K792088); AORTIC OCCLUDER; MULTIPLE UMBILICAL
Classification Name: DEVICE, OCCLUSION, UMBILICAL
Product Code: FOD
Device Class: 1
Regulation Number: 880.5950
Medical Specialty: General Hospital
Registered Establishment Name: Teleflex LLC (NADC)
Registered Establishment Number: 3010041511
Owner/Operator: Teleflex
Owner/Operator Number: 9062981
Establishment Operations: Manufacturer; Repackager/Relabeler
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