DORO LUCENT® Parallelogram Adaptor

GUDID 04250435520918

DORO LUCENT® Parallelogram Adaptor for Visius iMRI Systems

pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Skull clamp

• Primary Device ID: 04250435520918
• NIH Device Record Key: 01776ec2-6df7-42aa-9a31-e258d4320664
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DORO LUCENT® Parallelogram Adaptor
• Version Model Number: 4003.411
• Company DUNS: 313517922
• Company Name: pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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	04250435520918 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K063494

FDA Product Code

• HBL: Holder, Head, Neurosurgical (Skull Clamp)

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-15

On-Brand Devices [DORO LUCENT® Parallelogram Adaptor ]

• 04250435520918: DORO LUCENT® Parallelogram Adaptor for Visius iMRI Systems
• 04250435520390: DORO LUCENT® iMRI Parallelogram Adaptor MAQUET
• 04250435516287: DORO LUCENT® Parallelogram Adaptor TRUMPF for SIEMENS Aera/Skyra MRI Systems
• 04250435516256: DORO LUCENT® Parallelogram Adaptor MAQUET for SIEMENS Aera/Skyra MRI Systems