AIM (Advanced Imaging Modality) 0502-937-030

GUDID 07613327063912

HD Laparoscope, Autoclavable, 30 ¿ View Direction

STRYKER CORPORATION

Rigid optical laparoscope

• Primary Device ID: 07613327063912
• NIH Device Record Key: 7953ae4e-040a-4d55-bfa5-ecf984eb44e4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AIM (Advanced Imaging Modality)
• Version Model Number: 0502937030
• Catalog Number: 0502-937-030
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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

Customer Support Contacts

• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Dimensions

• Device Size Text, specify: 0
• Length: 33 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327063912 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142310

FDA Product Code

• OWN: Confocal optical imaging

Sterilization

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

[07613327063912]

Hydrogen Peroxide;Ethylene Oxide;Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [AIM (Advanced Imaging Modality)]

• 07613327063912: HD Laparoscope, Autoclavable, 30 ¿ View Direction
• 07613327063905: HD Laparoscope, Autoclavable, 0 ¿ View Direction
• 07613327059373: HD Laparoscope, Autoclavable, 30 ¿ View Direction
• 07613327059342: HD Laparoscope, Autoclavable, 0 ¿ View Direction