Clearview Black Belt Retractor Starter Set 7319-98T

GUDID 840199501724

Clearview Black Belt Retractor Starter Set Consists of the Following: Black Finish Stainless Steel Retractor Frames and Blue Finish Titanium Blades. 1x 7320-22T - Retractor frame Right 1x 7320-30T - Retractor frame Offset 2x 7320-40T - Blade Inserting Angled Clamps 2x 7322-34T - Pronged Blade Ti 34 mm, 2x 7322-40T - Pronged Blade Ti 40 mm, 2x 7322-45T - Pronged Blade Ti 45 mm, 2x 7322-50T - Pronged Blade Ti 50 mm, 2x 7322-55T - Pronged Blade Ti 55 mm, 2x 7322-60T - Pronged Blade Ti 60 mm, 2x 7324-34T - Blunt Blade Ti 34 mm, 2x 7324-40T - Blunt Blade Ti 40 mm, 2x 7324-45T - Blunt Blade Ti 45 mm, 2x 7324-50T - Blunt Blade Ti 50 mm, 2x 7324-55T - Blunt Blade Ti 55 mm, 2x 7324-60T - Blunt Blade Ti 60 mm, 1x 7319-90T - Sterilizing Instrument Case, 1.5 x 11 x 13"

KOROS U.S.A., INC.

Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable Self-retaining surgical retractor, reusable

• Primary Device ID: 840199501724
• NIH Device Record Key: 37b44e79-b497-4850-8342-77b7daae0bd9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clearview Black Belt Retractor Starter Set
• Version Model Number: 7319-98T
• Catalog Number: 7319-98T
• Company DUNS: 007928633
• Company Name: KOROS U.S.A., INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• 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

Customer Support Contacts

• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com
• Phone: 1-805-529-0825
• Email: customerservice@korosUSA.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature
• Special Storage Condition, Specify: Between 0 and 0 *Store in dry place at room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	10840199501721 [Primary]
GS1	840199501724 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K935529

FDA Product Code

• GZT: Retractor, Self-Retaining, For Neurosurgery

Sterilization

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

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

[840199501724]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-06
• Device Publish Date: 2021-06-28

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