Primary Device ID | 30382902206904 |
NIH Device Record Key | 5771b8ba-b4ff-43a4-8e27-86b0e5a140c0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD BBL Polyester Fiber-Tipped Applicator Swab |
Version Model Number | 220690 |
Catalog Number | 220690 |
Company DUNS | 122561087 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 1000 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 00382902206903 [Unit of Use] |
GS1 | 30382902206904 [Primary] |
LIO | Device, specimen collection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2018-05-25 |
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00382906651334 - Horizon | 2024-10-22 CD40 (5C3) BV605 ASR |