FDA UDI In Commercial Distribution 🇺🇸 United States

MICROPRIME

DI: 00840481135309 · Model: 90-00251 · Zest Anchors, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
MICROPRIME
Primary DI
00840481135309
Version / Model
90-00251
Company Name
Zest Anchors, LLC
Labeler DUNS
078387192
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2026-03-10
Public Version
1
Public Version Date
2026-03-18
Public Version Status
New
Public Device Record Key
c8883db2-8959-4ce5-8f98-4a3324cfad43

Device Description

Black Flocked Tip, 22 gauge

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EID Syringe, Restorative And Impression Material

GMDN Terms

Code Name
60366 Dental material injection cannula, single-use

Identifiers

Type ID
Primary 00840481135309
Unit of Use 10840481135306

Customer Contacts