Inami & Co., Ltd. M-171R

GUDID 00813059019752

Forceps Suturing and Tying Ultra Fine,- Forceps without teeth

Diamatrix

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

• Primary Device ID: 00813059019752
• NIH Device Record Key: 7c8166fb-a6c2-438c-a0c1-88144ed8242f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Inami & Co., Ltd.
• Version Model Number: M-171R
• Catalog Number: M-171R
• Company DUNS: 809555139
• Company Name: Diamatrix
• Device Count: 1
• DM Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813059019752 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

[00813059019752]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-15
• Device Publish Date: 2023-11-07

On-Brand Devices [Inami & Co., Ltd.]

• 00813059018502: Tanito Micro Hook for Trabeculotomy, Ab Interno, Left
• 00813059018496: Tanito Micro Hook for Trabeculotomy, Ab Interno, Right
• 00813059018489: Tanito Micro Hook for Trabeculotomy, Ab Interno, Straight
• 00813059019783: Forceps Cornea MISHIMA Original Model
• 00813059019776: Scissors Spring Handle Type Curved Short Pointed
• 00813059019769: Forceps Cornea and Suturing Type C Ultra Fine 0.12mm
• 00813059019752: Forceps Suturing and Tying Ultra Fine,- Forceps without teeth