LOW TORQUE INDICATING RATCHET WRENCH

GUDID 05712821006561

A dental torque wrench for placement and adjustment of dental implants, abutments, abutment screw and prosthetic screws during oral surgery and prosthetic procedures.

Elos Medtech Pinol A/S

Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable Surgical torque wrench, reusable

• Primary Device ID: 05712821006561
• NIH Device Record Key: 8119ba85-59df-4a65-8d5e-23ea6e4f0a71
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOW TORQUE INDICATING RATCHET WRENCH
• Version Model Number: L-TIRW
• Company DUNS: 306155953
• Company Name: Elos Medtech Pinol A/S
• 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: 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	05712821006561 [Primary]
GS1	05712821006615 [Direct Marking]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

[05712821006561]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-07-23
• Device Publish Date: 2020-07-15

Devices Manufactured by Elos Medtech Pinol A/S

• 05712821000309 - Elos Accurate Hybrid Base H Engaging: 2024-04-25 The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific c
• 05712821000316 - Elos Accurate Hybrid Base H Engaging: 2024-04-25 The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific c
• 05712821000323 - Elos Accurate Hybrid Base H Engaging: 2024-04-25 The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific c
• 05712821000330 - Elos Accurate Hybrid Base H Engaging: 2024-04-25 The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific c
• 05712821002532 - Abutment Blank: 2024-04-25 The Abutment Blank is used in creation of a customized abutment. It has a pre-manufactured connection interface that fits direct
• 05712821002556 - Abutment Blank: 2024-04-25 The Abutment Blank is used in creation of a customized abutment. It has a pre-manufactured connection interface that fits direct
• 05712821002570 - Abutment Blank: 2024-04-25 The Abutment Blank is used in creation of a customized abutment. It has a pre-manufactured connection interface that fits direct
• 05712821007797 - Elos Accurate Hybrid Base H Engaging: 2024-04-25 The Elos Accurate Hybrid Base is a titanium base designed to interface with a dental implant and to support a patient-specific c