ReadyLance 804

GUDID 00732671008046

Blood lancet, single-use

Primary Device ID	00732671008046
NIH Device Record Key	338ad79e-4bc4-4323-99d1-3a299d2ee595
Commercial Distribution Discontinuation	2025-08-27
Commercial Distribution Status	In Commercial Distribution
Brand Name	ReadyLance
Version Model Number	804
Catalog Number	804
Company DUNS	016069284
Company Name	AMITY HOLDINGS, LLC
Device Count	1
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	true
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00732671008046 [Package] Contains: 10732671108040 Package: Chipboard Carton [100 Units] Discontinued: 2025-08-27 In Commercial Distribution
GS1	10732671108040 [Primary]
GS1	20732671208044 [Package] Package: Corrugate carton [10 Units] Discontinued: 2025-08-27 In Commercial Distribution
GS1	30732671308048 [Package] Contains: 20732671208044 Package: Corrugate carton [4 Units] Discontinued: 2025-08-27 In Commercial Distribution

FMK	Lancet, Blood

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
READYLANCE 85210090 4088975 Live/Registered	LI, QIAN 2011-01-04