Primary Device ID | 53885-273-02 |
NIH Device Record Key | bb1a5a80-3bc6-449d-a25e-7ae9cf5570f5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OneTouch Verio |
Version Model Number | 022-273 |
Catalog Number | 022-273 |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | true |
Phone | +1 8885673003 |
XX@XX.XX |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00353885007764 [Primary] |
GS1 | 20353885007768 [Package] Contains: 00353885007764 Package: Shipper case [48 Units] In Commercial Distribution |
NDC/NHRIC | 53885-273-02 [Secondary] |
NBW | System, Test, Blood Glucose, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-12-03 |
Device Publish Date | 2019-11-25 |
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53885-273-02 | OneTouch Verio®Level 3 Control Solution |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ONETOUCH VERIO 77510844 4112124 Live/Registered |
LIFESCAN IP HOLDINGS, LLC 2008-06-30 |