Joseph scissors, Premium Line 20-640-14

GUDID 04250676740748

straight, pointed 14.5 cm

Spiggle & Theis Medizintechnik GmbH

Nasal scissors

• Primary Device ID: 04250676740748
• NIH Device Record Key: bf1f2cc7-aae2-4625-9781-9c29ae08e480
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Joseph scissors, Premium Line
• Version Model Number: 20-640-14
• Catalog Number: 20-640-14
• 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
• 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	04250676740748 [Primary]

FDA Product Code

• KBD: SCISSORS, NASAL

Sterilization

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

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

[04250676740748]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-15
• Device Publish Date: 2024-01-05

On-Brand Devices [Joseph scissors, Premium Line]

• 04250676740755: curved, pointed 14.5 cm
• 04250676740748: straight, pointed 14.5 cm