Primary Device ID | 00763000026882 |
NIH Device Record Key | 6e40636d-ad7d-4b98-9818-79f55d5bae9b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KYPHON Express II KyphoPak Tray |
Version Model Number | KEX102EB |
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 (at max. 25°C / 77°F), dry place |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool (at max. 25°C / 77°F), dry place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000026882 [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 | 2019-02-27 |
Device Publish Date | 2019-01-27 |
00763000026967 | BONE TAMP KIT KEX202NB AF E2 20/2 |
00763000026943 | BONE TAMP KIT KEX202EB FF E2 20/2 OI |
00763000026936 | BONE TAMP KIT KEX152NB AF E2 15/2 |
00763000026912 | BONE TAMP KIT KEX152EB FF E2 15/2 OI |
00763000026905 | BONE TAMP KIT KEX102NB AF E2 10/2 |
00763000026882 | BONE TAMP KIT KEX102EB FF E2 10/2 OI |