Primary Device ID | 30382904203185 |
NIH Device Record Key | 6921a7de-637b-433a-991f-3c3786c8caaa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BD SurePrep™ Capillary Tubes- PRECALIBRATED |
Version Model Number | 420318 |
Catalog Number | 420318 |
Company DUNS | 122561087 |
Company Name | BECTON, DICKINSON AND COMPANY |
Device Count | 200 |
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 |
Phone | +1(800)638-8663 |
Technical_services@bd.com | |
Phone | +1(800)638-8663 |
Technical_services@bd.com |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 15 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382904203184 [Unit of Use] |
GS1 | 30382904203185 [Primary] |
GIO | TUBE, COLLECTION, CAPILLARY BLOOD |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2018-05-25 |
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