Primary Device ID | 04066916015398 |
NIH Device Record Key | a87abef9-23ae-4c24-af07-73501ec26f0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 10 ml 92 x 15 ml |
Version Model Number | 62.610.202 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 100 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04066916015398 [Unit of Use] |
GS1 | 04066916015404 [Primary] |
NNK | Container, Specimen Mailer And Storage, Non-Sterile |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-25 |
Device Publish Date | 2024-12-17 |
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