Mulit-Snare

GUDID 00813623011502

Multi-Snare Micro Set 2mm x 175cm

pfm medical mepro gmbh

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• Primary Device ID: 00813623011502
• NIH Device Record Key: ca1cd413-1a41-4735-ab90-ba60e298b9c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mulit-Snare
• Version Model Number: 147302
• Company DUNS: 318460524
• Company Name: pfm medical mepro gmbh
• 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: true
• 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: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com
• Phone: (760)758-8749
• Email: customerservice@pfmmedicalusa.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813623011502 [Package]; Contains: 04042301061805; Package: Case [25 Units]; In Commercial Distribution
GS1	04042301061805 [Primary]
GS1	04042301109590 [Package]; Contains: 04042301061805; Package: Case [30 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011783

FDA Product Code

• DXE: Catheter, Embolectomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-07-08
• Device Publish Date: 2017-05-15

Devices Manufactured by pfm medical mepro gmbh

• 00813623011533 - Multi-Snare: 2021-07-08 Multi-Snare Set 10mm x 125cm
• 00813623011540 - Multi-Snare: 2021-07-08 Multi-Snare Set 15mm x 125cm
• 00813623011557 - Multi-Snare: 2021-07-08 Multi-Snare Set 20mm x 125cm
• 00813623011502 - Mulit-Snare: 2021-07-08Multi-Snare Micro Set 2mm x 175cm
• 00813623011502 - Mulit-Snare: 2021-07-08 Multi-Snare Micro Set 2mm x 175cm
• 00813623011519 - Multi-Snare: 2021-07-08 Multi-Snare Micro Set 4mm x 175cm
• 00813623011526 - Multi-Snare: 2021-07-08 Multi-Snare Set 5mm x 125cm
• 00813623011564 - Multi-Snare: 2021-07-08 Multi-Snare Set 30mm x 125cm