Occlude Aerosol Articulation Marking 23g - Red 05320

GUDID 00310866000213

Red Aerosol articulation marking spray, 23 grams

PASCAL COMPANY, INC.

Dental articulation paste/solution

• Primary Device ID: 00310866000213
• NIH Device Record Key: 7cb5201b-d838-4e4b-8234-3bb02aad03a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Occlude Aerosol Articulation Marking 23g - Red
• Version Model Number: 05320
• Catalog Number: 05320
• Company DUNS: 009260217
• Company Name: PASCAL COMPANY, INC.
• 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: false
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 8004268051
• Email: pascal@pascaldental.com

Operating and Storage Conditions

• Handling Environment Temperature: Between 0 Degrees Fahrenheit and 122 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00310866000213 [Primary]

FDA Product Code

• EFH: Paper, Articulation

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: 2019-03-04
• Device Publish Date: 2019-01-30

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• 00310866002620 - KOIS KR-4 PACKER: 2024-06-12 RETRACTION CORD PACKER INSPIRED BY KOIS 2MM HEAD
• 00310866002637 - KOIS KR-5 PACKER: 2024-06-12 RETRACTION CORD PACKER INSPIRED BY KOIS 2.5MM HEAD
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