Aeton Medical

GUDID 00810063330583

Healing Cap 4.8mm X 3.5mm, Nar Conical

Aetonmedical LLC

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 00810063330583
• NIH Device Record Key: 7c1fa3eb-dc3d-4d76-813f-11a0d6e247e2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aeton Medical
• Version Model Number: BNCH483
• Company DUNS: 043000598
• Company Name: Aetonmedical LLC
• 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: true
• Lot Batch: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810063330583 [Primary]

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

[00810063330583]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-16
• Device Publish Date: 2020-11-11

On-Brand Devices [Aeton Medical]

• 00810063330583: Healing Cap 4.8mm X 3.5mm, Nar Conical
• 00810063330705: Healing Cap 6.0mm X 3.5mm, Reg Conical