Accessory: Protection cap for microforceps & microscissors. 1286.CAP3

GUDID 08717872004907

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

• Primary Device ID: 08717872004907
• NIH Device Record Key: 60189a42-a7e3-48c1-aac3-a772bc792ae7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Accessory: Protection cap for microforceps & microscissors.
• Version Model Number: 1286.CAP3
• Catalog Number: 1286.CAP3
• 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	08717872004907 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

[08717872004907]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-17
• Device Publish Date: 2021-02-09

On-Brand Devices [Accessory: Protection cap for microforceps & microscissors.]

• 08717872004907: 1286.CAP3
• 08717872004891: 1286.CAP3