MICRO ELITE 8302
GUDID 30841156101491
Micro Elite Snare 7mm
TELEFLEX INCORPORATED
Intravascular catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare Intravascular extraction catheter-snare| Primary Device ID | 30841156101491 |
| NIH Device Record Key | b057e61a-24e1-4593-8225-18a079f534fb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MICRO ELITE |
| Version Model Number | IPN913612 |
| Catalog Number | 8302 |
| Company DUNS | 002348191 |
| Company Name | TELEFLEX INCORPORATED |
| 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 | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM |
Device Dimensions
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
| Width | 7 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10841156101497 [Primary] |
| GS1 | 30841156101491 [Package] Contains: 10841156101497 Package: Box [1 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K070502
FDA Product Code
| MMX | Device, percutaneous retrieval |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-11-11 |
| Device Publish Date | 2019-06-11 |
On-Brand Devices [MICRO ELITE]
| 30841156101491 | Micro Elite Snare 7mm |
| 30841156101484 | Micro Elite Snare 4mm |
| 30841156101477 | Micro Elite Snare 2mm |
Trademark Results [MICRO ELITE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICRO ELITE 76167522 2679722 Dead/Cancelled |
Kyocera Corporation 2000-11-17 |
 MICRO ELITE 74164215 1730874 Dead/Cancelled |
Dahlberg, Inc. 1991-05-06 |
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