25ga DEX TIPS™ Morris ILM Forceps

GUDID 00817489026205

25ga DEX TIPS™ Morris ILM 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

• Primary Device ID: 00817489026205
• NIH Device Record Key: 950338a8-d123-4ab6-86ad-9816d3ad922d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 25ga DEX TIPS™ Morris ILM Forceps
• Version Model Number: CVF4033-25
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817489026205 [Unit of Use]
GS1	10817489026202 [Primary]

FDA Product Code

• HNR: Forceps, Ophthalmic

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-11-09
• Device Publish Date: 2020-11-01

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