Accutome Surgical

GUDID 00844685011131

Harman Mosquito Forceps, Straight, 20mm

MICROSURGICAL TECHNOLOGY, INC.

Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable Ophthalmic soft-tissue manipulation forceps, probe-like, reusable

• Primary Device ID: 00844685011131
• NIH Device Record Key: bafdfafe-7919-4e9f-86fe-de3c36008894
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Accutome Surgical
• Version Model Number: AF4130
• Company DUNS: 097824130
• Company Name: MICROSURGICAL TECHNOLOGY, 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: true
• 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	00844685011131 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

[00844685011131]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-22
• Device Publish Date: 2023-03-14

On-Brand Devices [Accutome Surgical]

• 00844685006472: Machat / Sinskey Lasik Spatula Double-Ended
• 00844685011131: Harman Mosquito Forceps, Straight, 20mm
• 00844685011124: Hartman Mosquito Forceps, Curved, 20mm