Primary Device ID | 00808232001068 |
NIH Device Record Key | f60d7fc5-e4ab-4360-88b2-afb8c75118ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aliquot |
Version Model Number | 2090-0505 |
Catalog Number | 2090-0505 |
Company DUNS | 149183167 |
Company Name | Stryker Corporation |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(610)640-1775 |
inst.stryker.cs@stryker.com | |
Phone | +1(610)640-1775 |
inst.stryker.cs@stryker.com |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Length | 15 Centimeter |
Storage Environment Temperature | Between 20 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 20 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00808232001068 [Primary] |
OAR | Injector, vertebroplasty (does not contain cement) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-12-20 |
00808232001228 | Directional Bone Tamp |
00808232001211 | Directional Bone Tamp |
00808232001150 | Side-Port Syringe |
00808232001068 | Plunger Delivery Kit |
00808232001051 | Syringe Delivery Kit |
00808232001037 | Plunger Delivery Kit |
00808232001020 | Syringe Delivery Kit |
30808232001137 | Flexible Extensions |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALIQUOT 97290885 not registered Live/Pending |
Sartorius Stedim North America Inc. 2022-03-02 |
ALIQUOT 87539430 5542833 Live/Registered |
AquaPhoenix Scientific, Inc. 2017-07-24 |
ALIQUOT 77328139 3705935 Live/Registered |
ORTHOVITA, INC. 2007-11-13 |
ALIQUOT 76226375 2938480 Live/Registered |
ORTHOVITA, INC. 2001-03-19 |