Primary Device ID | 04038917189705 |
NIH Device Record Key | 8b68eb4b-4778-41b6-aecc-25d35543a8e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tube 50ml, 115x28mm, PP |
Version Model Number | 62.559.010 |
Company DUNS | 388000270 |
Company Name | Sarstedt Aktiengesellschaft & Co.KG |
Device Count | 25 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |