Primary Device ID | 04038917260015 |
NIH Device Record Key | 0803b516-fec0-46db-9c85-9617c8d8ca9f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 5 ml, 75 x 13 mm , PP |
Version Model Number | 55.525.060 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 1000 |
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 | 04038917260008 [Primary] |
GS1 | 04038917260015 [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 | 2024-11-01 |
Device Publish Date | 2024-10-24 |
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