Mapping Suction Probe

GUDID 04250307602988

Mapping Suction Probe 3/90 monopolar

inomed Medizintechnik GmbH

Nerve-locating system probe, single-use

• Primary Device ID: 04250307602988
• NIH Device Record Key: ccfa69f8-9b07-4ea4-a464-83ded63d30e1
• Commercial Distribution Discontinuation: 2023-02-26
• Commercial Distribution Status: Not 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: false
• 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	04250307602988 [Primary]
GS1	14250307602985 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-02-28
• Device Publish Date: 2023-01-23

On-Brand Devices [Mapping Suction Probe]

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