SAFEGUARD® 82050/B

GUDID 10884450202545

Merit Medical Systems, Inc.

Femoral artery compression system, manual, single-use

• Primary Device ID: 10884450202545
• NIH Device Record Key: a8f7bebb-bca6-49b6-b1b0-7a51da57e5ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAFEGUARD®
• Version Model Number: 10884450202545
• Catalog Number: 82050/B
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 10
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450202548 [Unit of Use]
GS1	10884450202545 [Primary]

FDA Product Code

• KCY: TOURNIQUET, PNEUMATIC

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: 2025-04-30
• Device Publish Date: 2018-02-16

On-Brand Devices [SAFEGUARD®]

• 10884450284008: 10884450284008
• 20884450249073: 10884450249076
• 20884450249066: 10884450249069
• 00884450249031: 10884450249038
• 00884450249130: 10884450249137
• 10884450202545: 10884450202545