FDA UDI In Commercial Distribution 🇺🇸 United States

AgaMatrix

DI: 00385541971010 · Model: 8000-01971 · AgaMatrix, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
100

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Basic Information

Brand Name
AgaMatrix
Primary DI
00385541971010
Version / Model
8000-01971
Catalog Number
N/A
Company Name
AgaMatrix, Inc.
Labeler DUNS
156756129
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-01-06
Public Version
2
Public Version Date
2025-09-23
Public Version Status
Update
Public Device Record Key
8a9b250c-8817-4a43-8c18-598090f928aa

Device Description

Lancets, AgaMatrix, 100CT, 33Gauge

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

GMDN Terms

Code Name
45142 Blood lancing device tip

Identifiers

Type ID
Package 20385541971014
Primary 00385541971010
Package 30385541971011
Unit of Use 80385541971016

Customer Contacts