Henry Schein 1045702

GUDID 00304040120286

Rubber Dam Punch IV Type

HENRY SCHEIN, INC.

Rubber dam punch

• Primary Device ID: 00304040120286
• NIH Device Record Key: 38aca58b-f939-41c7-a771-5ddb459da356
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Henry Schein
• Version Model Number: 1045702
• Catalog Number: 1045702
• Company DUNS: 012430880
• Company Name: HENRY SCHEIN, INC.
• Device Count: 1
• 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: false
• Lot Batch: true
• 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	00304040120286 [Primary]

FDA Product Code

• EIE: DAM, RUBBER

Sterilization

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

[00304040120286]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-13
• Device Publish Date: 2020-01-03

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