AKRUS

GUDID 04260647940008

AKRUS GmbH & Co. KG

Ophthalmic instrument table, line-powered

• Primary Device ID: 04260647940008
• NIH Device Record Key: 4c43f482-423e-4a53-b54b-1b3aa607e16e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AKRUS
• Version Model Number: CZM IT760.i
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260647940008 [Primary]

FDA Product Code

• FWZ: Operating Room Accessories Table Tray

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: 2023-12-08
• Device Publish Date: 2023-11-30

On-Brand Devices [AKRUS]

• 04260647940008: CZM IT760.i
• 04260647946239: AK 106
• 04260647943573: Patient Support System LSCneo
• 04260647941562: SC 5010SEK
• 04260647941517: AK 5010MBS
• 04260647940015: CZM IT1060.i
• 04260647946352: AK480
• 04260647945744: AK 447
• 04260647945706: AK446
• 04260647945560: Doctor Stool ak 445
• 04260647945539: Doctor stool ak 445
• 04260647945515: AK 445