Primary Device ID | 27290108240904 |
NIH Device Record Key | ec4be519-0042-4722-b364-b88b24aa49a5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ID Adapter |
Version Model Number | 5070204 |
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 | 07290108240900 [Primary] |
GS1 | 27290108240904 [Package] Contains: 07290108240900 Package: [320 Units] In Commercial Distribution |
FMF | Syringe, Piston |
Steralize Prior To Use | true |
Device Is Sterile | true |
[27290108240904]
Ethylene Oxide
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Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2016-11-18 |
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