Primary Device ID | 05000223449193 |
NIH Device Record Key | 1b8ad7ef-b76a-49ec-b03e-00f90c4009cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LEUKOSTRIP 13X102MM CTN 50 |
Version Model Number | 66002880 |
Catalog Number | 66002880 |
Company DUNS | 216344051 |
Company Name | SMITH & NEPHEW MEDICAL LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 05000223449186 [Primary] |
GS1 | 05000223449193 [Package] Contains: 05000223449186 Package: Carton [50 Units] In Commercial Distribution |
GS1 | 05000223449209 [Package] Package: Case [4 Units] In Commercial Distribution |
MZR | Topical Approximation System |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-17 |
Device Publish Date | 2020-04-09 |
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