Micro Dilator Forceps, Bayonet, Straight Tip, 35mm WL

GUDID 00810009460213

MIZUHO AMERICA, INC.

Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00810009460213
• NIH Device Record Key: 3f2cd498-f121-44f2-b269-88556a22f259
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Micro Dilator Forceps, Bayonet, Straight Tip, 35mm WL
• Version Model Number: 07-868-07MA
• Company DUNS: 877624940
• Company Name: MIZUHO AMERICA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810009460213 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[00810009460213]

Moist Heat or Steam Sterilization

[00810009460213]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-12-17
• Device Publish Date: 2025-12-09

Devices Manufactured by MIZUHO AMERICA, INC.

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• 00810009460213 - Micro Dilator Forceps, Bayonet, Straight Tip, 35mm WL: 2025-12-17
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