Primary Device ID | 50382904063080 |
NIH Device Record Key | 2ae0d153-5e85-458c-b092-99f288c6c9c1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Epilor, BD Luer-Lok |
Version Model Number | 406308 |
Catalog Number | 406308 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | true |
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 |
Storage Environment Temperature | Between 20 Degrees Celsius and 25 Degrees Celsius |
Storage Environment Temperature | Between 20 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382904063085 [Primary] |
GS1 | 50382904063080 [Package] Contains: 00382904063085 Package: Case [10 Units] In Commercial Distribution |
CAZ | Anesthesia conduction kit |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2016-09-16 |
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