Biopsy Forceps 504300L

GUDID 20705032056103

BIOPSY FORCEPS 7F 104CM

CORDIS CORPORATION

Endomyocardial biopsy forceps, single-use

• Primary Device ID: 20705032056103
• NIH Device Record Key: 58d9b038-4dd9-409d-8b73-ff7c4820a0dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biopsy Forceps
• Version Model Number: 504300L
• Catalog Number: 504300L
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705032056106 [Primary]
GS1	20705032056103 [Package]; Contains: 10705032056106; Package: BOX [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K810849

FDA Product Code

• DWZ: DEVICE, BIOPSY, ENDOMYOCARDIAL

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-03
• Device Publish Date: 2021-01-26

On-Brand Devices [Biopsy Forceps ]

• 20705032056110: BIOPSY FORCEPS 5.5F STD 50CM
• 20705032056103: BIOPSY FORCEPS 7F 104CM
• 20705032056097: BIOPSY FORCEPS 5.5F STD 104CM