Primary Device ID | 27290108241123 |
NIH Device Record Key | 0ae799da-0903-40dd-b59e-783372ab9f57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vented Vial Adapter 20mm |
Version Model Number | 8073039 |
Company DUNS | 600267793 |
Company Name | WEST PHARMA. SERVICES IL, . LTD |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290108241129 [Primary] |
GS1 | 17290108241126 [Package] Contains: 07290108241129 Package: [150 Units] In Commercial Distribution |
GS1 | 27290108241123 [Package] Contains: 17290108241126 Package: [4 Units] In Commercial Distribution |
LHI | Set, I.V. Fluid Transfer |
Steralize Prior To Use | true |
Device Is Sterile | true |
[27290108241123]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-18 |
Device Publish Date | 2018-04-08 |
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