Footrest extension

GUDID 04260647940039

AKRUS GmbH & Co. KG

Ophthalmic instrument table, line-powered

• Primary Device ID: 04260647940039
• NIH Device Record Key: c124ec3c-7b92-4a7d-88f7-42506bfd3dbe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Footrest extension
• Version Model Number: 472.010003
• Company DUNS: 324099522
• Company Name: AKRUS GmbH & Co. KG
• 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: false
• Serial Number: true
• 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

Customer Support Contacts

• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de
• Phone: +494121791930
• Email: sales@akrus.de

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260647940039 [Primary]

FDA Product Code

• HRJ: Table, Instrument, Powered, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-08
• Device Publish Date: 2025-11-28

Devices Manufactured by AKRUS GmbH & Co. KG

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• 04260647940039 - Footrest extension: 2025-12-08
• 04260647940039 - Footrest extension: 2025-12-08
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