Primary Device ID | 05907506237112 |
NIH Device Record Key | 80ba8945-833a-414c-bb2d-cb1dc3fc9006 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medlance Plus, safety lancet |
Version Model Number | Universal, 21G 1.8mm |
Catalog Number | 7044 |
Company DUNS | 422528088 |
Company Name | HTL STREFA S A |
Device Count | 200 |
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 |
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