Primary Device ID | 56949517070658 |
NIH Device Record Key | d31e32bf-1e4e-49f3-b1b5-9c471971b42c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Twist Lancet(30G) |
Version Model Number | LF-TL-30 |
Company DUNS | 421330121 |
Company Name | Shandong Lianfa Medical Plastic Products CO.,LTD |
Device Count | 150 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06949517004313 [Primary] |
GS1 | 56949517070658 [Unit of Use] |
FMK | Lancet, Blood |
QRL | Multiple Use Blood Lancet For Single Patient Use Only |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-26 |
Device Publish Date | 2020-10-16 |
56949517070689 | Sterile Lancet for Single Use (Box of 500 lancets), rediation(gamma) sterilization |
56949517070665 | Sterile Lancet for Single Use (Box of 500 lancets), sterilized with Ethylene Oxide |
56949517070658 | Sterile Lancet for Single Use (Box of 150 lancets), sterilized with Ethylene Oxide |