EXEL Injection Plug with Cap 26539

GUDID 20020221265396

Injection Plug with Cap, Luer Lock

Exel International

Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector Intravenous line recessed-needle connector

• Primary Device ID: 20020221265396
• NIH Device Record Key: 7d2676d5-cef6-481f-9b30-cc8b050b1ccb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXEL Injection Plug with Cap
• Version Model Number: 26539
• Catalog Number: 26539
• Company DUNS: 180572216
• Company Name: Exel International
• Device Count: 50
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00020221265392 [Unit of Use]
GS1	10020221265399 [Primary]
GS1	20020221265396 [Package]; Contains: 10020221265399; Package: [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011405

FDA Product Code

• FPA: Set, Administration, Intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-11-08
• Device Publish Date: 2016-09-22

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