Sickle knife 50-311-23

GUDID 04250381858677

curved edge working length 22 cm, total length 25 cm

Spiggle & Theis Medizintechnik GmbH

Laryngeal knife

• Primary Device ID: 04250381858677
• NIH Device Record Key: 7a28e4de-c1eb-4205-9d6c-b4a2601da80a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sickle knife
• Version Model Number: 50-311-23
• Catalog Number: 50-311-23
• 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	04250381858677 [Primary]

FDA Product Code

• KTG: KNIFE, ENT

Sterilization

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

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

[04250381858677]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-05
• Device Publish Date: 2022-09-27

On-Brand Devices [Sickle knife]

• 04250381813126: pointed 19.5 cm
• 04250381813157: pointed, curved right
• 04250381813140: pointed, left curved
• 04250381813133: rounded
• 04250381858677: curved edge working length 22 cm, total length 25 cm
• 04250381858660: straight edge working length 22 cm, total length 25 cm
• 04250381856628: pointed, left curved, bayonet 27 cm
• 04250381855485: pointed, curved right, bayonet 27 cm
• 04250676723192: pointed, straight, bayonet 27 cm