X-FINE bipolar forceps, NON-STICK 80-150-20-E

GUDID 04250676735904

bayonet, straight tip, tip length 4 mm 0.4 mm wide, guide pin, 20 cm

Spiggle & Theis Medizintechnik GmbH

Endoscopic electrosurgical electrode, bipolar, reusable

• Primary Device ID: 04250676735904
• NIH Device Record Key: 8ec58138-aa76-43db-abbb-e09e42a10a16
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: X-FINE bipolar forceps, NON-STICK
• Version Model Number: 80-150-20-E
• Catalog Number: 80-150-20-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	04250676735904 [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

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

Moist Heat or Steam Sterilization

[04250676735904]

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 [X-FINE bipolar forceps, NON-STICK]

• 04250676735966: bayonet,downwards angled tip, tip length 4mm, 0.4 mm wide, guide pin, 23 cm
• 04250676735904: bayonet, straight tip, tip length 4 mm 0.4 mm wide, guide pin, 20 cm