Primary Device ID | 30382903936510 |
NIH Device Record Key | 8ad392a2-5fe7-4f82-bd7b-f41e93e7cca1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PIVO Pro Needle-free Blood Collection Device |
Version Model Number | 393651 |
Catalog Number | 393651 |
Company DUNS | 124987988 |
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 | 00382903936519 [Primary] |
GS1 | 30382903936510 [Package] Contains: 00382903936519 Package: Shelfpack [50 Units] In Commercial Distribution |
GS1 | 50382903936514 [Package] Contains: 00382903936519 Package: Case [4 Units] In Commercial Distribution |
JKA | Tubes, vials, systems, serum separators, blood collection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-17 |
Device Publish Date | 2024-10-09 |
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