Suction tube 10-300-10

GUDID 04250676733238

angled, cylindrical 1.0 mm, 9 cm

Spiggle & Theis Medizintechnik GmbH

Surgical irrigation/aspiration cannula, non-illuminating, reusable

• Primary Device ID: 04250676733238
• NIH Device Record Key: 22439945-80d2-4174-99aa-325ffd12d1cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suction tube
• Version Model Number: 10-300-10
• Catalog Number: 10-300-10
• 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	04250676733238 [Primary]

FDA Product Code

• JZF: TUBE, EAR SUCTION

Sterilization

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

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

Moist Heat or Steam Sterilization

[04250676733238]

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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• 04250676733320: angled, cylindrical 3.0 mm, 11 cm
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• 04250676733276: angled, cylindrical 1.5 mm, 9 cm
• 04250676733238: angled, cylindrical 1.0 mm, 9 cm
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