ULTRAWIRE® 300719
GUDID 10801741079983
ULTRAWIRE® One-Handed Breast Localization Device, 19g x 7cm needle
Bard Peripheral Vascular, Inc.
Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Imaging lesion localization marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable Radiological image marker, implantable| Primary Device ID | 10801741079983 |
| NIH Device Record Key | 14fb00f8-4f03-4e2e-8b27-3d03b30cccbb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ULTRAWIRE® |
| Version Model Number | 300719 |
| Catalog Number | 300719 |
| Company DUNS | 135057938 |
| Company Name | Bard Peripheral Vascular, Inc. |
| Device Count | 1 |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Needle Gauge | 19 Gauge |
| Needle Gauge | 19 Gauge |
| Needle Gauge | 19 Gauge |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
| Device Size Text, specify | 0 |
| Needle Gauge | 19 Gauge |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741079986 [Primary] |
| GS1 | 10801741079983 [Package] Contains: 00801741079986 Package: CA [10 Units] In Commercial Distribution |
FDA Product Code
| GDF | GUIDE, NEEDLE, SURGICAL |
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 | 2018-03-29 |
| Device Publish Date | 2016-09-15 |
On-Brand Devices [ULTRAWIRE®]
| 10801741079990 | ULTRAWIRE® One-Handed Breast Localization Device, 19g x 9cm needle |
| 10801741079983 | ULTRAWIRE® One-Handed Breast Localization Device, 19g x 7cm needle |
| 10801741079976 | ULTRAWIRE® One-Handed Breast Localization Device, 19g x 5cm needle |
Trademark Results [ULTRAWIRE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ULTRAWIRE 78650045 3341185 Live/Registered |
C. R. BARD, INC. 2005-06-14 |
 ULTRAWIRE 76450016 3055853 Dead/Cancelled |
Electec Ltd. 2002-09-16 |
 ULTRAWIRE 75770938 not registered Dead/Abandoned |
INTELLIGENCE NETWORK ONLINE, INC. 1999-08-09 |
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