Primary Device ID | 04038917994088 |
NIH Device Record Key | c8c39df7-0e6c-4aa2-b1ad-6875b86f60c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micro tube 0.5ml, PP |
Version Model Number | 72.730.303 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 500 |
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 | 04038917994064 [Primary] |
GS1 | 04038917994088 [Unit of Use] |
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 | 2024-10-01 |
Device Publish Date | 2024-09-23 |
04038917392372 | 72.730.091 |
04038917392341 | 72.730.090 |
04038917335027 | 72.785.002 |
04038917194471 | 72.730.031 |
04038917195560 | 72.785.005 |
04038917194600 | 72.730.711 |
04038917194532 | 72.730.107 |
04038917194525 | 72.730.106 |
04038917194518 | 72.730.105 |
04038917194495 | 72.730.100 |
04038917194464 | 72.730.030 |
04038917194440 | 72.730.028 |
04038917194433 | 72.730.027 |
04038917223652 | 72.730.026 |
04038917194426 | 72.730.025 |
04038917194419 | 72.730.024 |
04038917194389 | 72.730.009 |
04038917194358 | 72.730.006 |
04038917194341 | 72.730.005 |
04038917194327 | 72.730.003 |
04038917193467 | 72.698.200 |
04038917166287 | 72.785 |
04038917165730 | 72.699 |
04038917165723 | 72.698 |
04038917996570 | 72.730.306 |
04038917994248 | 72.730.305 |
04038917994088 | 72.730.303 |