ProShape Retreat Assortment Kit

GUDID 10810138822712

Endo Direct LLC

Rotary/reciprocating endodontic file/rasp, reusable

• Primary Device ID: 10810138822712
• NIH Device Record Key: fa9783f8-bc6c-4c17-bde7-02f2b8928750
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProShape Retreat Assortment Kit
• Version Model Number: PSRTK
• Company DUNS: 125216703
• Company Name: Endo Direct LLC
• Device Count: 1
• DM Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10810138822712 [Primary]

FDA Product Code

• EKS: File, Pulp Canal, Endodontic

Sterilization

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

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

[10810138822712]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-29
• Device Publish Date: 2024-01-19

Devices Manufactured by Endo Direct LLC

• 10810138823276 - RC Mix: 2025-03-11
• 10810138823269 - ProShape Orifice Barrier: 2025-01-21
• 10810138823245 - ProShape Path Size 13 21mm: 2024-11-22
• 10810138823252 - ProShape Path Size 13 25mm: 2024-11-22
• 10810138823238 - EndoCeramic Root Repair Material: 2024-10-29
• 10810138822736 - ProShape Gutta Percha F1: 2024-08-12
• 10810138822743 - ProShape Gutta Percha F2: 2024-08-12
• 10810138822750 - ProShape Gutta Percha F3: 2024-08-12