Suction tip

GUDID 38033178018730

SORIN GROUP ITALIA SRL

Surgical/emergency suction cannula, non-illuminating, single-use

• Primary Device ID: 38033178018730
• NIH Device Record Key: 2e54ea3e-312a-4cbf-8150-554abb08353a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Suction tip
• Version Model Number: SU-22702
• Company DUNS: 442126587
• Company Name: SORIN GROUP ITALIA SRL
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033178018739 [Primary]
GS1	38033178018730 [Package]; Contains: 08033178018739; Package: BOX [10 Units]; In Commercial Distribution

FDA Product Code

• DTS: Sucker, cardiotomy return, cardiopulmonary bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-12
• Device Publish Date: 2024-04-04

On-Brand Devices [Suction tip]

• 38033178018754: SU-29602
• 38033178018747: SU-26702
• 38033178018730: SU-22702
• 38033178018723: SU-20802
• 38033178018716: SU-20602
• 38033178018709: SU-20601
• 38033178018679: SU-12502
• 38033178018662: SU-12402
• 38033178018655: SU-12202
• 38033178018648: SU-10101