Primary Device ID | 04066916016487 |
NIH Device Record Key | f90921c0-2f5b-40ff-89c1-c309d5692e2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 4 ml, 75 x 12 mm, K3E |
Version Model Number | 36.338.101 |
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 | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04066916016487 [Unit of Use] |
GS1 | 04066916016494 [Primary] |
PPM | General Purpose Reagent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-12 |
Device Publish Date | 2024-12-04 |
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