Dalrin Burnout Plastic Abutment Non Hex

GUDID 07290112443953

Dalrin Burnout Plastic Abutment Non Hex

ETGAR - MEDICAL INSTRUMENTS LTD

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 07290112443953
• NIH Device Record Key: 2367a0d6-fcc1-4470-9d7a-95b5f378fcc1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dalrin Burnout Plastic Abutment Non Hex
• Version Model Number: EIO-8123
• Company DUNS: 514570324
• Company Name: ETGAR - MEDICAL INSTRUMENTS LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290112443953 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-12-07
• Device Publish Date: 2018-03-04

On-Brand Devices [Dalrin Burnout Plastic Abutment Non Hex ]

• 07290112443953: Dalrin Burnout Plastic Abutment Non Hex
• 07290112443922: Dalrin Burnout Plastic Abutment Non Hex