Primary Device ID | 10884450404055 |
NIH Device Record Key | c1807f35-9424-4202-81a2-1e86c719ae1e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SafeSheath® Worley |
Version Model Number | 00884450404058 |
Catalog Number | FCL-200-03 |
Company DUNS | 065673912 |
Company Name | Merit Medical |
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 | 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 | false |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450404058 [Primary] |
GS1 | 10884450404055 [Package] Contains: 00884450404058 Package: [5 Units] In Commercial Distribution |
DYB | INTRODUCER, CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-07 |
Device Publish Date | 2019-12-30 |
10884450162313 | 00884450162316 |
10884450162306 | 00884450162309 |
10884450162290 | 00884450162293 |
10884450162283 | 00884450162286 |
10884450404055 | 00884450404058 |