Primary Device ID | 15903999602274 |
NIH Device Record Key | 99f17b3b-88a1-4162-b251-0816c4959106 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Droplet Acti-Lance, safety lancets |
Version Model Number | 28G x 1.5mm |
Catalog Number | 9630 |
Company DUNS | 422528088 |
Company Name | HTL STREFA S A |
Device Count | 50 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
50096295142995 - LEADER, pen needles | 2024-01-25 LEADER pen needles are sterile, single-use pen needles intended for use with pen injector devicec for the subcutaneous injection |
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The device |
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