Primary Device ID | 50382903008655 |
NIH Device Record Key | bee6359c-f330-4f89-bb1f-d9083128794f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD Plastipak Syringe |
Version Model Number | 300865 |
Catalog Number | 300865 |
Company DUNS | 001292192 |
Company Name | BECTON, DICKINSON AND COMPANY |
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 | true |
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 | 00382903008650 [Primary] |
GS1 | 30382903008651 [Package] Contains: 00382903008650 Package: Shelfpack [60 Units] In Commercial Distribution |
GS1 | 50382903008655 [Package] Contains: 30382903008651 Package: Case [4 Units] In Commercial Distribution |
FMF | Syringe, piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-06 |
Device Publish Date | 2024-05-29 |
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