Surgery-set PROGRESSIVE-LINE Flex J5300.0081

GUDID E219J530000811

Surgery-set PROGRESSIVE-LINE Flex

ALTATEC GmbH

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

• Primary Device ID: E219J530000811
• NIH Device Record Key: e963e5fc-3204-4bbc-adc8-035510c357f1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgery-set PROGRESSIVE-LINE Flex
• Version Model Number: J5300.0081
• Catalog Number: J5300.0081
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E219J530000811 [Primary]

FDA Product Code

• EJL: Bur, Dental

Sterilization

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

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

[E219J530000811]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-11
• Device Publish Date: 2025-04-03

Devices Manufactured by ALTATEC GmbH

• E219J508133091 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.3 mm, L 9 mm
• E219J508133111 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.3 mm, L 11 mm
• E219J508133131 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.3 mm, L 13 mm
• E219J508133161 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.3 mm, L 16 mm
• E219J508138071 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.8 mm, L 7 mm
• E219J508138091 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.8 mm, L 9 mm
• E219J508138111 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.8 mm, L 11 mm
• E219J508138131 - Guide dense bone drill 2, PL: 2025-05-21 Guide dense bone drill 2 PL, Ø 3.8 mm, L 13 mm