Device
RightLance Blood Lancing System
Manufacturer
TRUE INTEGRAL INC
Model: 28GI DI: 00860015786890 Status: New MRI: Labeling does not contain MRI Safety Information Single-use: Yes Rx: No OTC: No
First Published: 2026-05-28 Current Version: 2026-06-05
Description
RightLance Blood Lancing System
Sterilization
Device Sterile: Yes
Sterilization Prior To Use: No
Regulatory & Distribution
Record Status: Published
Version Number: 1
Record Key: 80d0bdb5-495a-4d21-b3e6-ea07bd7ca348
Distribution Status: In Commercial Distribution
DUNS Number: 117033737
Device Count: 10
DM Exempt: No
Premarket Exempt: No
HCT/P: No
Kit: No
Combination Product: No
Lot/Batch Tracked: Yes
Serial Number Tracked: No
Manufacturing Date Tracked: No
Expiration Date Tracked: Yes
Donation ID Number Tracked: Yes
Labeled Contains NRL: No
Labeled No NRL: No
Identifiers
Item #1 - Device ID: 10860015786897
Item #1 - Device ID Type: Unit of Use
Item #1 - Device ID Issuing Agency: GS1
Item #2 - Device ID: 00860015786890
Item #2 - Device ID Type: Primary
Item #2 - Device ID Issuing Agency: GS1
GMDN
Code: 61579
Name: Blood lancet, single-use
Definition:
A sterile, hand-held, sharply-pointed, non-mechanical, scalpel-like instrument intended to be used by a healthcare provider to manually puncture the skin of a patient to obtain a small blood specimen or drain a cyst or boil. This is a single-use device.
FDA Product Codes
QRK
Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature