Primary Device ID | 20353885010010 |
NIH Device Record Key | aee8f17d-5282-47a9-99e4-fc16ad1249df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OneTouch Ultra2 |
Version Model Number | 022-965 |
Catalog Number | 022-965 |
Company DUNS | 480240820 |
Company Name | LifeScan Europe GmbH |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
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 | true |
Phone | +1(800)227-8862 |
XX@XX.XX |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Handling Environment Temperature | Between 43 Degrees Fahrenheit and 111 Degrees Fahrenheit |
Handling Environment Temperature | Between 43 Degrees Fahrenheit and 111 Degrees Fahrenheit |
Handling Environment Temperature | Between 43 Degrees Fahrenheit and 111 Degrees Fahrenheit |
Handling Environment Temperature | Between 43 Degrees Fahrenheit and 111 Degrees Fahrenheit |
Handling Environment Temperature | Between 43 Degrees Fahrenheit and 111 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00353885010016 [Primary] |
GS1 | 20353885010010 [Package] Contains: 00353885010016 Package: Shipper case [10 Units] In Commercial Distribution |
NDC/NHRIC | 53885-296-01 [Secondary] |
NBW | SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-07-26 |
Device Publish Date | 2017-09-13 |
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