Adult Renal Clamps – Right KS-2002

GUDID B033KS20020

Adult Renal Clamps – Right

Kapp Surgical Instrument Co.

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

• Primary Device ID: B033KS20020
• NIH Device Record Key: e026e398-5e62-412f-87c5-9d51b067f40f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Adult Renal Clamps – Right
• Version Model Number: KS-2002
• Catalog Number: KS-2002
• Company DUNS: 004171112
• Company Name: Kapp Surgical Instrument Co.
• 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: true
• 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
HIBCC	B033KS20020 [Primary]

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

[B033KS20020]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-15
• Device Publish Date: 2023-06-07

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