Primary Device ID | 10709078008631 |
NIH Device Record Key | b4a250c7-bbca-4f5c-9cf2-e4c851182eaf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vented Luer Tip Cap |
Version Model Number | 0405 |
Company DUNS | 092673953 |
Company Name | WESTMED, INC. |
Device Count | 500 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00709078008627 [Primary] |
GS1 | 10709078008631 [Unit of Use] |
JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-25 |
Device Publish Date | 2020-05-15 |
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