Biopsy Punches, Sterile, 8.0 mm, Purple

GUDID 00840117323667

DYNAREX CORPORATION

Skin-coring punch, single-use

• Primary Device ID: 00840117323667
• NIH Device Record Key: cd9357f5-f9b2-4220-b92e-4f9494981c79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biopsy Punches, Sterile, 8.0 mm, Purple
• Version Model Number: 4096
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840117322813 [Primary]
GS1	00840117322950 [Package]; Contains: 00840117322813; Package: Case [24 Units]; In Commercial Distribution
GS1	00840117323667 [Unit of Use]

FDA Product Code

• LRY: Punch, Surgical

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: 2022-05-31
• Device Publish Date: 2022-05-23

On-Brand Devices [Biopsy Punches, Sterile, 8.0 mm, Purple]

• 00840117323667: 4096
• 00840117340923: 4096