Aufricht Nasal Rasp 07-050-45

GUDID G25007050450

A hand-held manual surgical instrument with a surface(s) of coarse and/or fine grooves or teeth designed to scrape and smooth the surface of bone during a surgical procedure. The device is typically a one-piece instrument with grooves/teeth along all or part of its working end(s). It is available in a variety of sizes and working end designs, including straight and curved ends and often double-ended with a central handle. It is not dedicated for use at a specific anatomy (e.g., sinus, ear) and it is made of metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device.

N S SURGICAL COMPANY

Bone file/rasp, manual, reusable

• Primary Device ID: G25007050450
• NIH Device Record Key: e9a13623-8aeb-48c3-acbd-76ba99a7b80d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aufricht Nasal Rasp
• Version Model Number: 07-050-45
• Catalog Number: 07-050-45
• Company DUNS: 645681649
• Company Name: N S SURGICAL COMPANY
• 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: false
• OTC Over-The-Counter: false

Device Dimensions

• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter
• Length: 18.5 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G25007050450 [Primary]

FDA Product Code

• KBA: Rasp, Nasal

Sterilization

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

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25007050450]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-05
• Device Publish Date: 2023-04-27

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