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U.S. Department of Health and Human Services

Establishment Registration & Device Listing
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Proprietary Name: Biopsy Forceps
Classification Name: TUBING, PUMP, CARDIOPULMONARY BYPASS
Product Code: DWE
Device Class: 2
Regulation Number: 870.4390
Medical Specialty: Cardiovascular
Registered Establishment Name: CORDIS CORPORATION
Registered Establishment Number: 1016427
Owner/Operator: CORDIS CORPORATION
Owner/Operator Number: 1016427
Establishment Operations: Manufacturer; Specification Developer; Complaint File Establishment
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