Primary Device ID | 00850014448004 |
NIH Device Record Key | 4c145367-78d4-48ec-8c07-a1cf1229e93f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VACSURE SAFETY MULTI-SAMPLE NEEDLE |
Version Model Number | VM-1021 |
Catalog Number | VM-1021 |
Company DUNS | 117338398 |
Company Name | LABOTEK GROUP CORP |
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 | 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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00850014448004 [Primary] |
GS1 | 10850014448001 [Package] Package: Inner Box [50 Units] In Commercial Distribution |
GS1 | 20850014448008 [Package] Contains: 10850014448001 Package: Case [10 Units] In Commercial Distribution |
FMF | Syringe, Piston |
FMI | Needle, Hypodermic, Single Lumen |
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 | 2021-02-01 |
Device Publish Date | 2021-01-23 |
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