TIPCAM

GUDID 04048551416174

TIPCAM®1 S 3D, 45°, 4 mm

Karl Storz GmbH & Co. KG

Rigid optical neuroscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable

• Primary Device ID: 04048551416174
• NIH Device Record Key: 95297434-1574-4049-8a15-4ec5647c47c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TIPCAM
• Version Model Number: 28164FA3D
• Company DUNS: 315731430
• Company Name: Karl Storz GmbH & Co. KG
• 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: true
• Manufacturing Date: false
• 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	04048551416174 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162880

FDA Product Code

• GWG: Endoscope, neurological

Sterilization

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

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

[04048551416174]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-10
• Device Publish Date: 2020-03-02

Devices Manufactured by Karl Storz GmbH & Co. KG

• 04048438000984 - n.a.: 2024-03-19 Patient Tubing Set, for day sets
• 04048438001042 - n.a.: 2024-03-19 Tubing Set, UNIDRIVE/UNIDRIVE SIII
• 04048438001233 - n.a.: 2024-03-19 Gas filter, gas flow 30 l/min
• 04048438002230 - n.a.: 2024-03-19 Tubing Set, CLEARVISION II (irrigation)
• 04048438002964 - n.a.: 2024-03-19 Tubing Set, ARTHROPUMP Power(irrigation)
• 04048438003176 - n.a.: 2024-03-19 Pump Tubing Day Set
• 04048438005316 - n.a.: 2024-03-19 Insufflation Tubing Set, with gas filter
• 04048438005330 - n.a.: 2024-03-19 Insufflation tubing set, ENDOFLATOR 50