Desmarres Chalazion Forceps 20mm/9cm 06-008-09

GUDID G25006008090

A hand-held manual instrument designed primarily for non-dedicated grasping of devices, sponges and/or dressings during a procedure; it is neither intended for tissue manipulation nor endoscopic use. It typically has a tweezers-like design with two blades joined at the proximal (non-working) end with variously designed tips at the working end. It is made of metal and/or plastic materials and is available in various sizes. This is a reusable device intended to be sterilized prior to use.

N S SURGICAL COMPANY

Dressing/utility forceps, tweezers-like, reusable

• Primary Device ID: G25006008090
• NIH Device Record Key: 1b02b074-28f2-4437-b9c3-46bf276247b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Desmarres Chalazion Forceps 20mm/9cm
• Version Model Number: 06-008-09
• Catalog Number: 06-008-09
• 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: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter
• Length: 9 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G25006008090 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25006008090]

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: 2023-04-05
• Device Publish Date: 2023-03-28

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