Fisch footplate elevator 10-643-02

GUDID 04250676735409

90°, upwards, angled shaft 0.3 mm, 16 cm

Spiggle & Theis Medizintechnik GmbH

ENT elevator

• Primary Device ID: 04250676735409
• NIH Device Record Key: 2d2d0775-e143-4330-836f-50359f3e7d2e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fisch footplate elevator
• Version Model Number: 10-643-02
• Catalog Number: 10-643-02
• Company DUNS: 332893028
• Company Name: Spiggle & Theis Medizintechnik GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676735409 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676735409]

Moist Heat or Steam Sterilization

[04250676735409]

Moist Heat or Steam Sterilization

[04250676735409]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-19
• Device Publish Date: 2025-09-11

On-Brand Devices [Fisch footplate elevator]

• 04250676735416: 90°, downwards, angled shaft 0.3 mm, 16 cm
• 04250676735409: 90°, upwards, angled shaft 0.3 mm, 16 cm