R-55A Circlet Packing Instrument 26140

GUDID 00310866000688

Retraction Cord Packing Instrument, Circlet off Angle, Serrated Tip

PASCAL COMPANY, INC.

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• Primary Device ID: 00310866000688
• NIH Device Record Key: 04a101ce-1330-47bc-abc3-029dd3d8a0aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: R-55A Circlet Packing Instrument
• Version Model Number: 26140
• Catalog Number: 26140
• Company DUNS: 009260217
• Company Name: PASCAL COMPANY, 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: 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

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00310866000688 [Primary]

FDA Product Code

• EIF: Accessories, Retractor, Dental

Sterilization

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

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

[00310866000688]

High-level Disinfectant;Moist Heat or Steam Sterilization;Dry Heat Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-01
• Device Publish Date: 2019-01-29

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