Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth,Bayonet, Round Handle, 210mm

GUDID 00840096215229

Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth, Bayonet, Round Handle, 210mm | Kogent

KATALYST SURGICAL LLC

Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable Surgical soft-tissue manipulation forceps, tweezers-like, reusable

• Primary Device ID: 00840096215229
• NIH Device Record Key: c33f28d4-a339-4ae6-81f3-96dc824fe3f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth,Bayonet, Round Handle, 210mm
• Version Model Number: N4403
• Company DUNS: 007883297
• Company Name: KATALYST SURGICAL LLC
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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	00840096215229 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

[00840096215229]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-26
• Device Publish Date: 2024-06-18

On-Brand Devices [Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth,Bayonet, Round Handle, 210mm]

• 00840096212440: Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth, Bayonet, Round Handle, 210mm | Kogent
• 00840096215229: Straight Forceps, 0.5mmTips, Interlocking 1x2 Teeth, Bayonet, Round Handle, 210mm | Kogent