Primary Device ID | 10840935101802 |
NIH Device Record Key | 43c9b896-cbaf-43da-99d8-287e1859e5e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | All Purpose Cuff |
Version Model Number | 98-0084-71 |
Company DUNS | 148191133 |
Company Name | SUNTECH MEDICAL, 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 | false |
Lot Batch | false |
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 | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com | |
Phone | +1-919-654-2300 |
UDI_MAIL@suntechmed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10840935101802 [Primary] |
DXQ | Blood Pressure Cuff |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2016-09-12 |