Knife 50-313-23

GUDID 04250381858691

round, 45° angled, 2,5 mm working length 22 cm, total length 25 cm

Spiggle & Theis Medizintechnik GmbH

Laryngeal knife

• Primary Device ID: 04250381858691
• NIH Device Record Key: fde88d1d-300f-43d4-8b49-b4030931c128
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Knife
• Version Model Number: 50-313-23
• Catalog Number: 50-313-23
• 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	04250381858691 [Primary]

FDA Product Code

• KTG: KNIFE, ENT

Sterilization

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

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

Moist Heat or Steam Sterilization

[04250381858691]

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 [Knife]

• 04250381858714: golf club shaped working length 22 cm, total length 25 cm
• 04250381858707: oval, vertical wl 22 cm, tl 25 cm
• 04250381858691: round, 45° angled, 2,5 mm working length 22 cm, total length 25 cm
• 04250381858684: oval, straight working length 22 cm, total length 25 cm
• 04250676735072: straight, lanceolate 23 cm