20GA Aspirating Laser Probe, SMA906

GUDID 10632307002158

20GA Aspirating Laser Probe, SMA906

PEREGRINE SURGICAL, LTD.

Ophthalmic laser system beam guide

• Primary Device ID: 10632307002158
• NIH Device Record Key: c528964d-b7fb-4667-a646-c368c2232464
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 20GA Aspirating Laser Probe, SMA906
• Version Model Number: GA-0040013
• Company DUNS: 622467348
• Company Name: PEREGRINE SURGICAL, LTD.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: ryan@peregrine-surgical.com

Device Dimensions

• Needle Gauge: 20 Gauge
• Needle Gauge: 20 Gauge
• Needle Gauge: 20 Gauge
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge
• Device Size Text, specify: 0
• Needle Gauge: 20 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00632307002151 [Primary]
GS1	10632307002158 [Package]; Contains: 00632307002151; Package: Box [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061024

FDA Product Code

• HQF: Laser, ophthalmic

Sterilization

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

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

[10632307002158]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-01

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