Primary Device ID | 36945630121013 |
NIH Device Record Key | 9190647d-7573-498a-b6b2-c962825f4773 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Telli Health |
Version Model Number | 01-0130 |
Company DUNS | 554434897 |
Company Name | Sterilance Medical (Suzhou) Inc. |
Device Count | 25 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06945630121012 [Unit of Use] |
GS1 | 16945630121019 [Primary] |
GS1 | 36945630121013 [Package] Contains: 16945630121019 Package: [400 Units] In Commercial Distribution |
QRK | Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-08 |
Device Publish Date | 2023-08-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TELLI HEALTH 98416884 not registered Live/Pending |
ACCUHEALTH TECHNOLOGIES, LLC 2024-02-22 |
TELLI HEALTH 90191930 not registered Live/Pending |
ACCUHEALTH TECHNOLOGIES, LLC 2020-09-18 |
TELLI HEALTH 90191881 not registered Live/Pending |
ACCUHEALTH TECHNOLOGIES, LLC 2020-09-18 |