Mapping Suction Probe

GUDID 14250307611413

Mapping Suction Probe 3/90, Monopolar

inomed Medizintechnik GmbH

Nerve-locating system probe, single-use

• Primary Device ID: 14250307611413
• NIH Device Record Key: e545e333-4808-434d-addd-87624d3ebd20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mapping Suction Probe
• Version Model Number: 525650
• Company DUNS: 340782259
• Company Name: inomed Medizintechnik GmbH
• Device Count: 4
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	04250307611416 [Primary]
GS1	14250307611413 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K212164

FDA Product Code

• ETN: Stimulator, Nerve

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-07
• Device Publish Date: 2023-02-27

On-Brand Devices [Mapping Suction Probe]

• 04250307602988: Mapping Suction Probe 3/90 monopolar
• 14250307611413: Mapping Suction Probe 3/90, Monopolar