Temporary Cylinder MUATCL

GUDID 08806388244102

Ø4.8 / L=10

Megagen Implant Co. Ltd

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 Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 08806388244102
• NIH Device Record Key: f010527e-678b-4e48-9f70-e1f1f7969bb2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Temporary Cylinder
• Version Model Number: MUATC
• Catalog Number: MUATCL
• Company DUNS: 687388178
• Company Name: Megagen Implant Co. Ltd
• 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: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806388244102 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203808

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

[08806388244102]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-11-26
• Device Publish Date: 2021-11-18

On-Brand Devices [Temporary Cylinder]

• 08806388203512: AnyRidge Internal Ø5.8/ Octa
• 08806388203505: AnyRidge Internal Ø4.8/ Octa
• 08806388203499: AnyRidge Internal Ø3.8/ Octa
• 08806388203482: AnyRidge Internal Ø5.8/ Non-Octa
• 08806388203475: AnyRidge Internal Ø4.8/ Non-Octa
• 08806388203468: AnyRidge Internal Ø3.8/ Non-Octa
• 08806388244102: Ø4.8 / L=10