Multi-Snare
GUDID 00813623011557
Multi-Snare Set 20mm x 125cm
pfm medical mepro gmbh
Intravascular extraction catheter-snare| Primary Device ID | 00813623011557 |
| NIH Device Record Key | 79d3a2bc-ad82-4dd7-9ab8-a46156d40af4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Multi-Snare |
| Version Model Number | 147320 |
| 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 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com | |
| Phone | (760)758-8749 |
| customerservice@pfmmedicalusa.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813623011557 [Package] Contains: 04042301033604 Package: Case [25 Units] In Commercial Distribution |
| GS1 | 04042301033604 [Primary] |
| GS1 | 04042301033611 [Package] Contains: 04042301033604 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 |
On-Brand Devices [Multi-Snare]
| 00813623011564 | Multi-Snare Set 30mm x 125cm |
| 00813623011526 | Multi-Snare Set 5mm x 125cm |
| 00813623011519 | Multi-Snare Micro Set 4mm x 175cm |
| 00813623011557 | Multi-Snare Set 20mm x 125cm |
| 00813623011540 | Multi-Snare Set 15mm x 125cm |
| 00813623011533 | Multi-Snare Set 10mm x 125cm |
Trademark Results [Multi-Snare]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTI-SNARE 87104586 5146285 Live/Registered |
PFM Medical, Inc. 2016-07-14 |
 MULTI-SNARE 86523415 not registered Dead/Abandoned |
PFM MEDICAL, INC. 2015-02-03 |
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