DORO LUCENT® Transitional Member

GUDID 04250435521755

DORO LUCENT® Locking Transitional Member

pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Skull clamp

• Primary Device ID: 04250435521755
• NIH Device Record Key: 83dcb7e7-3995-477a-b511-6fc628da9344
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DORO LUCENT® Transitional Member
• Version Model Number: 1101.031
• 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: 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	04250435521755 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032331

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® Transitional Member ]

• 04250435521762: DORO LUCENT® Transitional Member Spine, Radiolucent
• 04250435521755: DORO LUCENT® Locking Transitional Member
• 04250435521748: DORO LUCENT® Transitional Member