Primary Device ID | 00850007350147 |
NIH Device Record Key | b8efa250-6077-4e3c-be86-dc5053181aaf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | T/Pump |
Version Model Number | TP700C |
Company DUNS | 116981210 |
Company Name | C2DX, 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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850007350147 [Primary] |
ILO | Pack, Hot Or Cold, Water Circulating |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-11 |
Device Publish Date | 2022-05-03 |
00850007350147 | T/pump Professional |
00850007350130 | T/pump Professional |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() T/PUMP 73132579 1095062 Live/Registered |
GAYMAR INDUSTRIES, INC. 1977-07-01 |