RAD11161

GUDID 10888551039482

FEMORAL COMPRESSION SYSTEM FEMOSTOP PLUS HD -- HEMOSTATIC DRESSING NOT INCLUDED --

STERILMED, INC.

Femoral artery compression system, manual, single-use

• Primary Device ID: 10888551039482
• NIH Device Record Key: 7d39d1e9-625f-4ea3-8822-f199bbf4b48b
• Commercial Distribution Discontinuation: 2019-04-17
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: RAD11161
• Catalog Number: RAD11161
• Company DUNS: 175899459
• Company Name: STERILMED, 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)541-0078
• Email: customerservice@sterilmed.com
• Phone: +1(888)541-0078
• Email: customerservice@sterilmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10888551039482 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120204

FDA Product Code

• NMF: Clamp, vascular, reprocessed

Sterilization

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

[10888551039482]

Ethylene Oxide

[10888551039482]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2019-04-17
• Device Publish Date: 2016-09-22

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• 10888551045209 - NA: 2021-10-20 REPROCESSED PENTARAY NAV ECO HIGH DENSITY MAPPING CATHETER, D CURVE
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• 10888551021531 - NA: 2021-01-22 KNIVES (1) HOOK BLADE (1) TRIANGLE BLADE ENDOTRAC BLADE SYSTEM
• 10888551000048 - NA: 2020-11-06 CTS RELIEF KIT, 5PC SET
• 10888551012928 - NA: 2020-10-19 ENDO LUNG