25ga OEM DEX™ Super Grip Forceps

GUDID 10817489026851

25ga OEM DEX™ Super Grip Forceps

KATALYST SURGICAL LLC

Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use Ophthalmic soft-tissue manipulation forceps, probe-like, single-use

• Primary Device ID: 10817489026851
• NIH Device Record Key: 01dbaa7b-940b-44db-801b-26b7e5564c17
• Commercial Distribution Discontinuation: 2023-04-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: 25ga OEM DEX™ Super Grip Forceps
• Version Model Number: DVFO4034-25
• Company DUNS: 007883297
• Company Name: KATALYST SURGICAL LLC
• Device Count: 5
• 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: 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817489026854 [Unit of Use]
GS1	10817489026851 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-04-27
• Device Publish Date: 2017-12-19

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