GUDID 00840682118019

GE Healthcare Austria GmbH & Co OG

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00840682118019
• NIH Device Record Key: 3b13ff87-2ba8-4df6-a7b1-a2f0a01a171c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: RAB2-5L
• Company DUNS: 300599979
• Company Name: GE Healthcare Austria GmbH & Co OG
• 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: 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	00840682118019 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041688

FDA Product Code

• IYO: System, imaging, pulsed echo, ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-07-15

Devices Manufactured by GE Healthcare Austria GmbH & Co OG

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• 00195278699800 - Voluson: 2023-11-15 Voluson Expert 18 BT24
• 00195278699824 - Voluson: 2023-11-15 Voluson Expert 20 BT24
• 00195278283375 - RIC10-D: 2023-10-19 RIC10-D
• 00195278347473 - Voluson: 2022-08-24 Voluson Expert 18
• 00195278347480 - Voluson: 2022-08-24 Voluson Expert 20
• 00195278347497 - Voluson: 2022-06-22 Voluson Expert 22