Primary Device ID | 00763000031886 |
NIH Device Record Key | b4ba9253-4ec7-4732-9624-7c1d2eb8b889 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BALLOON KYPHOPLASTY ESSENTIALS |
Version Model Number | NH153PB |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, 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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000031886 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-26 |
Device Publish Date | 2019-01-26 |
00763000031893 | KIT NH203PB 20/3 SPINE ESSEN FF |
00763000031886 | KIT NH153PB 15/3 SPINE ESSEN FF |
00763000031879 | KIT NH152PB 15/2 SPINE ESSEN FF |
00763000031862 | KIT NH103PB 10/3 SPINE ESSEN FF |
00763000031855 | KIT NH102PB 10/2 SPINE ESSEN FF |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BALLOON KYPHOPLASTY ESSENTIALS 86934265 5443850 Live/Registered |
Warsaw Orthopedic, Inc. 2016-03-09 |