Dunn Dautrey osteotome 20-444-08

GUDID 04250676741752

slightly curved 8 mm, 17 cm

Spiggle & Theis Medizintechnik GmbH

Plastic surgery osteotome

• Primary Device ID: 04250676741752
• NIH Device Record Key: 66f5816b-c1e5-4bf9-ab30-c10f0a7f5090
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dunn Dautrey osteotome
• Version Model Number: 20-444-08
• Catalog Number: 20-444-08
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676741752 [Primary]

FDA Product Code

• GFI: OSTEOTOME, MANUAL

Sterilization

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

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

[04250676741752]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-06
• Device Publish Date: 2025-09-26

On-Brand Devices [Dunn Dautrey osteotome]

• 04250676741783: strongly curved 8 mm, 17 cm
• 04250676741776: strongly curved 6 mm, 17 cm
• 04250676741769: strongly curved 4 mm, 17 cm
• 04250676741752: slightly curved 8 mm, 17 cm
• 04250676741745: slightly curved 6 mm, 17 cm
• 04250676741738: slightly curved 4 mm, 17 cm
• 04250676741721: straight 8 mm, 17 cm
• 04250676741714: straight 6 mm, 17 cm
• 04250676741707: straight 4 mm, 17 cm