Primary Device ID | 15019517155006 |
NIH Device Record Key | 4f16fb35-4cc3-4f8b-963c-3eb306a1ee9a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CADD |
Version Model Number | 21-2112-0402-51L |
Company DUNS | 082005361 |
Company Name | Smiths Medical ASD, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15019517155006 [Primary] |
PYR | Neuraxial Administration Set - Intrathecal delivery |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-09 |
Device Publish Date | 2020-02-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CADD 85113149 4025048 Dead/Cancelled |
Smiths Medical ASD, Inc. 2010-08-23 |
CADD 78847519 3201977 Live/Registered |
SMITHS MEDICAL ASD, INC. 2006-03-28 |
CADD 75656568 2554554 Dead/Cancelled |
NOBEL BIOCARE AB 1999-03-08 |
CADD 73751005 1547216 Live/Registered |
PHARMACIA DELTEC, INC. 1988-09-07 |
CADD 73661271 1686787 Dead/Cancelled |
AUDIO ANALYSTS INC. 1987-05-18 |
CADD 73062204 1070788 Dead/Cancelled |
Ready Stamping System Inc. 1975-09-05 |