Connection Cable

GUDID 04260463848960

Aktormed GmbH

Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder Surgical camera holder

• Primary Device ID: 04260463848960
• NIH Device Record Key: c1bb4d6a-9799-4d6b-a1a2-3ebfc5993110
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connection Cable
• Version Model Number: 171896
• Company DUNS: 537223815
• Company Name: Aktormed GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]
GS1	04260463848960 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473
• Premarket Notification: K200473

FDA Product Code

• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument
• NAY: System, Surgical, Computer Controlled Instrument

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: 2021-02-22
• Device Publish Date: 2021-02-12

Devices Manufactured by Aktormed GmbH

• 04260463848823 - Headset Voice Control: 2021-02-22
• 04260463848946 - Voice Control: 2021-02-22
• 04260463848953 - Y-Cord: 2021-02-22
• 04260463848960 - Connection Cable: 2021-02-22
• 04260463848960 - Connection Cable: 2021-02-22
• 04260463849141 - Voice Control Set: 2021-02-22 Set consiting of: 1x Voice Control (171894 1x Headset (171882) 1x Power Cord C13 1x Y-line (171895) 1x Connection Cable (171896
• 04260463840353 - Power Supply: 2019-10-22
• 04260463840544 - SUPPLY CABLE: 2019-10-22
• 04260463843392 - TENSION SLEEVE 10mm: 2019-10-22