Dolphin

GUDID EIBAE30620201

T2D Mini Varian

IBA Dosimetry GmbH

Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer Radiation electrometer

• Primary Device ID: EIBAE30620201
• NIH Device Record Key: 238faf19-a567-4d7b-ad01-9d6c3a0acdc8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dolphin
• Version Model Number: E3062020
• Company DUNS: 332599307
• Company Name: IBA Dosimetry 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: 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

Customer Support Contacts

• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com
• Phone: +49912860738
• Email: service@iba-group.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EIBAE30620200 [Primary]
HIBCC	EIBAE30620201 [Package]; Contains: EIBAE30620200; Package: Transport case [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072374

FDA Product Code

• IYE: Accelerator, Linear, Medical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-09

On-Brand Devices [Dolphin]

• EIBAE30620281: T2D Mini Elekta EU
• EIBAE30620271: T2D Mini Varian EU
• EIBAE30620251: T2D Mini Elekta Korea
• EIBAE30620241: T2D Mini Varian Korea
• EIBAE30620211: T2D Mini Elekta
• EIBAE30620201: T2D Mini Varian