Monopolar Forceps 50-400-23

GUDID 04250381858882

Monopolar coagulation forceps, rotatable, serrated, straight, smoke evacuation, shaft 3.0 mm, 23.5 cm

Spiggle & Theis Medizintechnik GmbH

Endoscopic electrosurgical electrode, monopolar, reusable

• Primary Device ID: 04250381858882
• NIH Device Record Key: e4b48271-fcda-4ac9-a8de-bf9ee5ce2f1e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monopolar Forceps
• Version Model Number: 50-400-23
• Catalog Number: 50-400-23
• Company DUNS: 332893028
• Company Name: Spiggle & Theis Medizintechnik GmbH
• 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: true
• 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

Customer Support Contacts

• Phone: +492206908153
• Email: p.stockmann@spiggle-theis.com

Device Dimensions

• Length: 23.5 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250381858882 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101080

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[04250381858882]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-06-17
• Device Publish Date: 2019-06-07

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