DORO® Transitional Member

GUDID 04250435503829

DORO® Transitional Member long-modified

pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung

Skull clamp

• Primary Device ID: 04250435503829
• NIH Device Record Key: 7c1fcc58-189b-4a31-aa9d-9d12a572729a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DORO® Transitional Member
• Version Model Number: 4001-15
• 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: true
• Serial Number: false
• 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	04250435503829 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001808

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® Transitional Member]

• 04250435510100: DORO® Transitional Member Radiolucent, Bracing
• 04250435503850: DORO® Transitional Member Radiol. long
• 04250435503843: DORO® Transitional Member Radiol. short
• 04250435503829: DORO® Transitional Member long-modified
• 04250435502006: DORO® Transitional Member RDL (to ALU Base Unit)
• 04250435500453: Transitional Member Teflon coated US