MI Intercostal Retractor System (IRS) 222 Medium Blade Set MI-IRS-MB-P01

GUDID 00858733006093

The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory components include a retractor rack, 4 different sized paired blade set options, 2 different sized double swivel blade options and a custom sterilization tray.

Biorep Technologies, Inc.

Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00858733006093
• NIH Device Record Key: 6e523392-cddf-41c7-aba3-35d5550397ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MI Intercostal Retractor System (IRS) 222 Medium Blade Set
• Version Model Number: 3.0
• Catalog Number: MI-IRS-MB-P01
• Company DUNS: 073724333
• Company Name: Biorep Technologies, Inc.
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00858733006093 [Primary]

FDA Product Code

• DWS: Instruments, Surgical, Cardiovascular

Sterilization

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

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

[00858733006093]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-01
• Device Publish Date: 2024-04-23

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