Primary Device ID | 56949517070108 |
NIH Device Record Key | ea89441a-4d6d-4799-b523-a7942f79c209 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Safety lancet PAII(23G) |
Version Model Number | LF-PAII-23 |
Company DUNS | 421330121 |
Company Name | Shandong Lianfa Medical Plastic Products CO.,LTD |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |