Universal ventilation tube inserter 10-758-00

GUDID 04250676730725

irrigation channel

Spiggle & Theis Medizintechnik GmbH

Tympanostomy tube inserter, reusable

• Primary Device ID: 04250676730725
• NIH Device Record Key: 55463f85-c204-473f-81a2-76bfecc7fb49
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Universal ventilation tube inserter
• Version Model Number: 10-758-00
• Catalog Number: 10-758-00
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250676730725 [Primary]

FDA Product Code

• LRC: INSTRUMENT, ENT MANUAL SURGICAL

Sterilization

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

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

[04250676730725]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-03
• Device Publish Date: 2025-09-25

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• 04250676711625 - Fork: 2025-10-07 curved 10.5 cm
• 04250676716880 - ENT-single-use suction tubes, angled: 2025-10-07 transparent, Luer-Lock 130 x 2.0 mm, sterile, box of 50
• 04250676716897 - ENT-single-use suction tubes, angled: 2025-10-07 blue, Luer-Lock 130 x 3.0 mm, sterile, box of 50
• 04250676731982 - Salivary duct probe: 2025-10-07 straight, cylindrical 0.5 mm diameter
• 04250676731999 - Salivary duct probe: 2025-10-07 straight, cylindrical 0.6 mm diameter
• 04250676732002 - Salivary duct probe: 2025-10-07 straight, cylindrical 0.8 mm diameter