Hoffmann ear forceps 10-279-00

GUDID 04250381847121

throughcutting, round 2.5 mm, 8 cm

Spiggle & Theis Medizintechnik GmbH

Surgical soft-tissue manipulation forceps, alligator, reusable

• Primary Device ID: 04250381847121
• NIH Device Record Key: 995fef57-c6e0-4b7f-9127-c60d4bb624c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hoffmann ear forceps
• Version Model Number: 10-279-00
• Catalog Number: 10-279-00
• 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	04250381847121 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

Moist Heat or Steam Sterilization

[04250381847121]

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

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• 04250676715821: throughcutting, round, straight 2.0 mm, 8 cm
• 04250676702654: throughcutting, oval 1.8x3.4 mm, 8 cm
• 04250381847121: throughcutting, round 2.5 mm, 8 cm
• 04250676741967: throughcutting, oval 8 cm