Primary Device ID | 30732671308062 |
NIH Device Record Key | 0f4ae2ea-08ba-4b49-9bfb-63ab4e99c543 |
Commercial Distribution Discontinuation | 2025-06-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ReadyLance |
Version Model Number | 806 |
Catalog Number | 806 |
Company DUNS | 016069284 |
Company Name | AMITY HOLDINGS, LLC |
Device Count | 100 |
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 | true |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com | |
Phone | 8003278894 |
wconety@medicore.com |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Needle Gauge | 21 Gauge |
Length | 2.2 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00732671008060 [Primary] |
GS1 | 10732671108064 [Unit of Use] |
GS1 | 20732671208068 [Package] Contains: 00732671008060 Package: Corrugate Carton [10 Units] Discontinued: 2025-06-01 In Commercial Distribution |
GS1 | 30732671308062 [Package] Contains: 20732671208068 Package: Corrugate Carton [4 Units] Discontinued: 2025-06-01 In Commercial Distribution |
FMK | Lancet, Blood |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-08-28 |
Device Publish Date | 2020-06-01 |
30732671308086 | Safety Lancet |
30732671308062 | Safety Lancet |
30732671308055 | Safety Lancet |
30732671308031 | Safety Lancet |
30732671308024 | Safety Lancet |
00732671008169 | Safety Lancet |
00732671008091 | Safety Lancet |
00732671008046 | Safety Lancet |
20732671208013 | Safety Lancet |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
READYLANCE 85210090 4088975 Live/Registered |
LI, QIAN 2011-01-04 |