Primary Device ID | 20353885011574 |
NIH Device Record Key | 154cc125-d63a-48ee-81b1-87feb8a45ac3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OneTouch Ultra Blue |
Version Model Number | 011-424 |
Catalog Number | 011-424 |
Company DUNS | 480240820 |
Company Name | LifeScan Europe GmbH |
Device Count | 10 |
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 | 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 | true |
Phone | +1(800)227-8862 |
XX@XX.XX |
Special Storage Condition, Specify | Between 0 and 0 *Store your test strips in their original vial only. |
Special Storage Condition, Specify | Between 0 and 0 *Store your test strips in their original vial only. |
Special Storage Condition, Specify | Between 0 and 0 *Store your test strips in their original vial only. |
Special Storage Condition, Specify | Between 0 and 0 *Store your test strips in their original vial only. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00353885011570 [Primary] |
GS1 | 20353885011574 [Package] Contains: 00353885011570 Package: Shipper case [450 Units] In Commercial Distribution |
GS1 | 80353885011576 [Unit of Use] |
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 | 3 |
Public Version Date | 2019-07-26 |
Device Publish Date | 2017-09-13 |
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20353885004187 | OneTouch Ultra Test Strips Blue for blood glucose testing with: OneTouch Ultra 2, OneTouch Ultra |