Kerrison rongeur 10-416-02

GUDID 04250676716453

size 2, dismountable 4.5 mm, 10 cm

Spiggle & Theis Medizintechnik GmbH

Craniofacial rongeur, reusable

• Primary Device ID: 04250676716453
• NIH Device Record Key: af544bfc-3fab-4f32-b560-48e2599f6a65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kerrison rongeur
• Version Model Number: 10-416-02
• Catalog Number: 10-416-02
• 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
• 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	04250676716453 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

Moist Heat or Steam Sterilization

[04250676716453]

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 [Kerrison rongeur]

• 04250676716460: size 3, dismountable 5.0 mm, 10 cm
• 04250676716453: size 2, dismountable 4.5 mm, 10 cm
• 04250676716446: size 1, dismountable 4.0 mm, 10 cm
• 04250381846476: size 2, dismountable 4.5 mm, 10 cm
• 04250676717351: size 0, dismountable 3.5 mm