AccessGUDID - DEVICE: CareLiving Pressure Activated Safety lancet 26G (00383568100246)

GUDID

Device Identifier (DI) Information

Brand Name: CareLiving Pressure Activated Safety lancet 26G
Version or Model: Activated Safety Lancet 26
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 83568-1002-46
Company Name: Care Living Diagnostics Inc.

Primary DI Number: 00383568100246
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 100
Labeler D-U-N-S® Number*: 125354643 *Terms of Use

Device Description: Pressure Activated Safety lancet 26G*1.8mm,100pcs Per Box,Sterile Singel-use,No need pre-loading,High speed of penetration and low puncture force provide users an almost painless experience of blood sampling.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	Yes
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
61578	Manual blood lancing device, single-use	A sterile, hand-held manual instrument intended to be used for controlled skin puncture/cut to obtain a capillary blood specimen, performed by a healthcare provider (e.g., on a neonate) or a patient (e.g., a diabetic), typically at the fingertip or ear lobe. It includes a preloaded lancet tip, and has a manually-powered mechanism (e.g., spring-loaded) which enables the tip to puncture to a predetermined depth and blood subsequently to be squeezed out of the puncture site. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Needle Gauge: 28 Gauge

Device Record Status

Public Device Record Key: a6f90913-e880-437f-8b2b-c16bf475cc57
Public Version Date: July 04, 2024
Public Version Number: 1
DI Record Publish Date: June 26, 2024