Bipolar forceps, NON-STICK 80-106-19

GUDID 04250381887868

straight, angled tip, tip length 8 mm 1.0 mm wide, guide pin, 19.5 cm

Spiggle & Theis Medizintechnik GmbH

Endoscopic electrosurgical electrode, bipolar, reusable

• Primary Device ID: 04250381887868
• NIH Device Record Key: e6da12b6-1c46-4ab3-8df5-82f0a3a3f903
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bipolar forceps, NON-STICK
• Version Model Number: 80-106-19
• Catalog Number: 80-106-19
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com
• Phone: +492206908165
• Email: c.winterschladen@spiggle-theis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250381887868 [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

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

[04250381887868]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-06
• Device Publish Date: 2022-09-28

On-Brand Devices [Bipolar forceps, NON-STICK]

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• 04250381889794: straight, angled tip, tip length 8 mm 1.0 mm wide, guide pin, 16 cm
• 04250676735935: bayonet, tip length 8 mm, 0.7 mm wide guide pin, 25 cm
• 04250381888001: bayonet, tip length 8 mm, 1.2 mm wide guide pin, 25 cm
• 04250381887868: straight, angled tip, tip length 8 mm 1.0 mm wide, guide pin, 19.5 cm