Primary Device ID | 10891153001733 |
NIH Device Record Key | 890afee9-3eab-424d-859f-2b4260acd271 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tempo |
Version Model Number | 8050 |
Company DUNS | 009046405 |
Company Name | Hemasource, Inc. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00891153001736 [Primary] |
GS1 | 10891153001733 [Package] Contains: 00891153001736 Package: Case [10 Units] In Commercial Distribution |
LKB | Pad, Alcohol, Device Disinfectant |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
[10891153001733]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-18 |
Device Publish Date | 2022-12-08 |
10891153001733 | Tempo BZK Towelette |
10891153001184 | Tempo Alcohol Prep Pads (Sterile) |