23GA Membrane Scraper

GUDID 10632307000031

23GA Membrane Scraper

PEREGRINE SURGICAL, LTD.

General-purpose ophthalmic hook, single-use General-purpose ophthalmic hook, single-use

• Primary Device ID: 10632307000031
• NIH Device Record Key: bc24f1a0-8c97-4830-ae30-33fabdf6805e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 23GA Membrane Scraper
• Version Model Number: PD800.23
• Company DUNS: 622467348
• Company Name: PEREGRINE SURGICAL, LTD.
• 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: 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: jayne@peregrine-surgical.com
• Phone: +1(215)348-0456
• Email: jayne@peregrine-surgical.com

Device Dimensions

• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge
• Needle Gauge: 23 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00632307000034 [Primary]
GS1	10632307000031 [Package]; Contains: 00632307000034; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Sterilization

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

[10632307000031]

Ethylene Oxide

[10632307000031]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-05-06

On-Brand Devices [23GA Membrane Scraper]

• 10632307000031: 23GA Membrane Scraper
• 00632307002274: 23GA Membrane Scraper