Subretinal cannula, curved 20 gauge/0.9 mm needle with 0.3 mm tip. 1295.3

GUDID 08717872006840

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

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable

• Primary Device ID: 08717872006840
• NIH Device Record Key: 19bfbf99-228c-42fa-9f06-cde3955bdfdd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Subretinal cannula, curved 20 gauge/0.9 mm needle with 0.3 mm tip.
• Version Model Number: 1295.3
• Catalog Number: 1295.3
• 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	08717872006840 [Primary]

FDA Product Code

• HMX: Cannula, Ophthalmic

Sterilization

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

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

[08717872006840]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-19
• Device Publish Date: 2021-02-11

On-Brand Devices [Subretinal cannula, curved 20 gauge/0.9 mm needle with 0.3 mm tip.]

• 08717872006840: 1295.3
• 08717872006833: 1295.3