Retrobulbar Needle - Sharp 1225

GUDID 08134650112256

For administrating local anesthetic agents prior to ophthalmic surgery.

HURRICANE MEDICAL INC

Hypodermic needle, single-use

• Primary Device ID: 08134650112256
• NIH Device Record Key: 375de3c7-b57f-4331-8483-1bc8cbe8e0b6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Retrobulbar Needle - Sharp
• Version Model Number: 1225
• Catalog Number: 1225
• Company DUNS: 093377724
• Company Name: HURRICANE MEDICAL INC
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Needle Gauge: 25 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	08134650112256 [Primary]

FDA Product Code

• GAA: Needle, Aspiration And Injection, Disposable

Sterilization

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

[08134650112256]

Ethylene Oxide;Radiation Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-28
• Device Publish Date: 2020-01-20

On-Brand Devices [Retrobulbar Needle - Sharp]

• 08134650112256: For administrating local anesthetic agents prior to ophthalmic surgery.
• 00813465010077: For administrating local anesthetic agents prior to ophthalmic surgery.