#11 – Micro Curette, Angled

GUDID 00840096204001

#11 – Micro Curette, Angled

KATALYST SURGICAL LLC

Bone curette, reusable Bone curette, reusable Bone curette, reusable

• Primary Device ID: 00840096204001
• NIH Device Record Key: 43c0b762-4ba6-45a5-8aa8-94308daf6229
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: #11 – Micro Curette, Angled
• Version Model Number: N090-080
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840096204001 [Primary]
GS1	00840096204001 [Primary]
GS1	00840096204001 [Primary]

FDA Product Code

• FZS: Curette, Surgical, General Use
• FZS: Curette, Surgical, General Use
• FZS: Curette, Surgical, General Use

Sterilization

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

[00840096204001]

Moist Heat or Steam Sterilization

[00840096204001]

Moist Heat or Steam Sterilization

[00840096204001]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-05-19
• Device Publish Date: 2020-05-11

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