Bite registration cap J2112.4310

GUDID E219J211243101

Bite registration cap, Ø 4.3 mm, PBT (6 units), sterile

ALTATEC GmbH

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 Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: E219J211243101
• NIH Device Record Key: 2aae41e2-fd6e-427d-a572-aad7a0927ecc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bite registration cap
• Version Model Number: J2112.4310
• Catalog Number: J2112.4310
• Company DUNS: 322018193
• Company Name: ALTATEC GmbH
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com
• Phone: 7609181857
• Email: info@camlog.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E219J211243101 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-26
• Device Publish Date: 2023-12-18

On-Brand Devices [Bite registration cap]

• E219J211260101: Bite registration cap, Ø 6.0 mm, PBT (6 units), sterile
• E219J211250101: Bite registration cap, Ø 5.0 mm, PBT (6 units), sterile
• E219J211243101: Bite registration cap, Ø 4.3 mm, PBT (6 units), sterile
• E219J211238101: Bite registration cap, Ø 3.8 mm, PBT (6 units), sterile
• E219J211233101: Bite registration cap, Ø 3.3 mm, PBT (6 units), sterile