Primary Device ID | 00616784705736 |
NIH Device Record Key | 2e8c73b3-70a6-43f8-884b-a0ff71597165 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dead End Stopper & Cap |
Version Model Number | 7057 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 200 |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784705712 [Unit of Use] |
GS1 | 00616784705729 [Primary] |
GS1 | 00616784705736 [Package] Contains: 00616784705729 Package: [2000 Units] In Commercial Distribution |
FMG | Stopcock, I.V. Set |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-12 |
Device Publish Date | 2018-10-10 |
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