Healing cap

GUDID 07640156471922

Thommen Medical AG

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 07640156471922
• NIH Device Record Key: 6d225875-395a-474a-aaad-07ecbca6a1d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Healing cap
• Version Model Number: 4.03.519
• Company DUNS: 481614829
• Company Name: Thommen Medical AG
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640156471922 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072649

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

[07640156471922]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-07
• Device Publish Date: 2015-10-24

On-Brand Devices [Healing cap]

• 07640156473667: 4.03.510
• 07640156473650: 4.03.511
• 07640156473643: 4.03.512
• 07640156473636: 4.03.513
• 07640156473629: 4.03.514
• 07640156471960: 4.03.515
• 07640156471953: 4.03.516
• 07640156471946: 4.03.517
• 07640156471939: 4.03.518
• 07640156471922: 4.03.519