Microforceps: Avci Foreign Body.(17 gauge / 1.5 mm) 2286.H

GUDID 08717872008660

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.

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: 08717872008660
• NIH Device Record Key: 81951c2e-6325-4d0e-8056-26000458e203
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Microforceps: Avci Foreign Body.(17 gauge / 1.5 mm)
• Version Model Number: 2286.H
• Catalog Number: 2286.H
• Company DUNS: 407522184
• Company Name: D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
• 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: false
• 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	08717872008660 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

[08717872008660]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-24
• Device Publish Date: 2021-02-11

On-Brand Devices [Microforceps: Avci Foreign Body.(17 gauge / 1.5 mm)]

• 08717872008677: 2286.H
• 08717872008660: 2286.H