AccessGUDID - DEVICE: Members Mark (MHC1732101)

GUDID

Device Identifier (DI) Information

Brand Name: Members Mark
Version or Model: 732101
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: MHC MEDICAL PRODUCTS, LLC

Primary DI Number: MHC1732101
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 100
Labeler D-U-N-S® Number*: 169895245 *Terms of Use

Device Description: The lancets are single use but the lancing device is a multiple use blood lancet for single patient use only.

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
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?
37243	Manual blood lancing device, reusable	A hand-held manual instrument intended to be used for controlled skin puncture to obtain a capillary blood specimen (e.g., performed by a diabetic patient) typically at the fingertip or ear lobe. It is used with a sterile, disposable 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 reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
QRL	Multiple Use Blood Lancet For Single Patient Use Only

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: No
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
No Device Sizes

Device Record Status

Public Device Record Key: 75976a88-362d-4d54-8b6a-3ab9332b9e03
Public Version Date: June 29, 2026
Public Version Number: 3
DI Record Publish Date: September 16, 2025