Tapered Suction Tube, 6Fr, Malleable, 13.3cm WL

GUDID 00810009466017

Suction Tube

MIZUHO AMERICA, INC.

Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable Surgical/emergency suction cannula, non-illuminating, reusable

• Primary Device ID: 00810009466017
• NIH Device Record Key: 8f76fc7d-34b6-4ecb-bc5d-e464aafd7d49
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tapered Suction Tube, 6Fr, Malleable, 13.3cm WL
• Version Model Number: 10224MA
• Company DUNS: 877624940
• Company Name: MIZUHO AMERICA, INC.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810009466017 [Primary]

FDA Product Code

• GEA: Cannula, Surgical, General & Plastic Surgery

Sterilization

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

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

[00810009466017]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-23
• Device Publish Date: 2023-08-15

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