Surgery set CERALOG® PROGRESSIVE-LINE Flex H5300.0070

GUDID E219H530000701

Surgery set CERALOG® PROGRESSIVE-LINE Flex

ALTATEC GmbH

Dental/maxillofacial surgical procedure kit, non-medicated, reusable

• Primary Device ID: E219H530000701
• NIH Device Record Key: de7d3af6-556c-4cef-89e1-4e8d74a72f6e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgery set CERALOG® PROGRESSIVE-LINE Flex
• Version Model Number: H5300.0070
• Catalog Number: H5300.0070
• 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: false
• 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: 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	E219H530000701 [Primary]

FDA Product Code

• EJL: Bur, Dental

Sterilization

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

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

[E219H530000701]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-27
• Device Publish Date: 2023-12-19

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• E219C242133201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.3 mm, L 20.0 mm, 2 units
• E219C242138201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.8 mm, L 20.0 mm, 2 units
• E219C242143201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 4.3 mm, L 20.0 mm, 2 units
• E219C242150201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 5.0 mm, L 20.0 mm, 2 units
• E219C244133201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.3 mm, L 20.0 mm, 2 units
• E219C244138201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 3.8 mm, L 20.0 mm, 2 units
• E219C244143201 - CONELOG® CAM Titan. Blank, type ME: 2024-06-06 CONELOG® CAM Titan. Blank, type ME, d 12 mm, d 4.3 mm, L 20.0 mm, 2 units