Pro Advantage P072523

GUDID M220P0725235

PA STOCKINETTE SYNTHETIC 3X25YD - (EA)

NATIONAL DISTRIBUTION & CONTRACTING, INC.

Stockinette

• Primary Device ID: M220P0725235
• NIH Device Record Key: f862279c-2243-4214-8aa4-0ac8e12aa9d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pro Advantage
• Version Model Number: P072523
• Catalog Number: P072523
• Company DUNS: 009831413
• Company Name: NATIONAL DISTRIBUTION & CONTRACTING, 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: true
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• 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 Identifiers

Device Issuing Agency	Device ID
HIBCC	M220P0725233 [Primary]
HIBCC	M220P0725235 [Package]; Contains: M220P0725233; Package: case [12 Units]; In Commercial Distribution

FDA Product Code

• IPM: Cover, Limb

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-05
• Device Publish Date: 2022-10-11

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• M220P5492405: Pro Advantage Cuff Bladder 2 Tube Large Adult Black Latex Free
• M220P5492203: Pro Advantage Cuff Bladder 2 Tube Adult Black Latex Free
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