Anderson Retractor 19cm Blunt 4x4 09-047-19

GUDID G25009047190

A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a reusable device.

N S SURGICAL COMPANY

Hand-held surgical retractor, reusable

• Primary Device ID: G25009047190
• NIH Device Record Key: 5c139612-e2a8-4309-8e69-ea6e8db1070a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Anderson Retractor 19cm Blunt 4x4
• Version Model Number: 09-047-19
• Catalog Number: 09-047-19
• 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: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter
• Length: 19 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G25009047190 [Primary]

FDA Product Code

• GAD: Retractor

Sterilization

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

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

Ethylene Oxide;Moist Heat or Steam Sterilization;Ultraviolet Light

[G25009047190]

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: 2023-05-08
• Device Publish Date: 2023-04-28

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