Langenbeck raspatory 10-348-19

GUDID 04250676710222

width 16 mm, 19.5 cm

Spiggle & Theis Medizintechnik GmbH

Bone file/rasp, manual, reusable

• Primary Device ID: 04250676710222
• NIH Device Record Key: 84d13063-fbc7-41b7-8c4a-1aa06cf76f73
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Langenbeck raspatory
• Version Model Number: 10-348-19
• Catalog Number: 10-348-19
• 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	04250676710222 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

[04250676710222]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-19
• Device Publish Date: 2022-09-09

On-Brand Devices [Langenbeck raspatory]

• 04250676710222: width 16 mm, 19.5 cm
• 04250676738387: 18 mm, 19.5 cm