Primary Device ID | 00847713000800 |
NIH Device Record Key | 52d324a1-6384-45f6-83ed-ddfe34b0b10c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | microdot® Pro Test Strips (25ct) |
Version Model Number | 400-25 |
Company DUNS | 962314360 |
Company Name | Cambridge Sensors USA LLC |
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 | true |
Manufacturing Date | false |
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 | 00847713000800 [Primary] |
GS1 | 00847713000848 [Unit of Use] |
LFR | Glucose Dehydrogenase, Glucose |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-07 |
Device Publish Date | 2024-10-30 |
00847713000800 - microdot® Pro Test Strips (25ct) | 2024-11-07microdot® Pro Test Strips (25ct) |
00847713000800 - microdot® Pro Test Strips (25ct) | 2024-11-07 microdot® Pro Test Strips (25ct) |
00847713000817 - microdot® Pro Test Strips (50ct) | 2024-11-07 microdot® Pro Test Strips (50ct) |
00847713000787 - microdot® Pro Glucometer | 2024-10-30 microdot® Pro Glucometer |
00847713000794 - microdot® Pro Control Solution | 2024-10-30 microdot® Pro Control Solution |
00847713000589 - microdot® | 2023-05-09 microdot® Pulse Oximeter |
00847713000510 - microdot | 2022-12-06 |
00847713000398 - microdot | 2022-12-01 Nitrile powder free examination gloves. |
00847713000411 - microdot | 2022-12-01 Nitrile powder free examination gloves. |