Grünwald-Henke punch 25-010-11

GUDID 04250676716309

size 1, straight 3.0 mm, 11.5 cm

Spiggle & Theis Medizintechnik GmbH

Bone-coring punch, reusable

• Primary Device ID: 04250676716309
• NIH Device Record Key: b5556714-bc9f-4c5a-b60f-e52acb97ad56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Grünwald-Henke punch
• Version Model Number: 25-010-11
• Catalog Number: 25-010-11
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676716309 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676716309]

Moist Heat or Steam Sterilization

[04250676716309]

Moist Heat or Steam Sterilization

[04250676716309]

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: 2025-09-28

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