Matrix Strip

GUDID D701MDS2

Dead soft matrix strip, (001”/.025 mm) 20’ roll

PULPDENT CORPORATION

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• Primary Device ID: D701MDS2
• NIH Device Record Key: 50be019e-939d-4fa9-a6e1-0d9db52bb9ec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Matrix Strip
• Version Model Number: M-DS
• Company DUNS: 001006089
• Company Name: PULPDENT CORPORATION
• 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: 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
HIBCC	D701MDS2 [Primary]

FDA Product Code

• JEP: Retainer, Matrix

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-30
• Device Publish Date: 2021-09-22

On-Brand Devices [Matrix Strip]

• D701MTP2: Transparent matrix strip, (002”/.05 mm) 59’ roll
• D701MDS2: Dead soft matrix strip, (001”/.025 mm) 20’ roll