Bipolar forceps, NON-STICK 80-125-07-E

GUDID 04250676735935

bayonet, tip length 8 mm, 0.7 mm wide guide pin, 25 cm

Spiggle & Theis Medizintechnik GmbH

Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable

• Primary Device ID: 04250676735935
• NIH Device Record Key: 55e0bc7c-5f58-443f-acfe-d1a5314695ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bipolar forceps, NON-STICK
• Version Model Number: 80-125-07-E
• Catalog Number: 80-125-07-E
• 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	04250676735935 [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

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

Moist Heat or Steam Sterilization

[04250676735935]

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]

• 04250381887905: Bipolar forceps, NON-STICK, bayonet, tip length 8 mm, 2.0 mm wide,guide pin, 16 cm
• 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