FDA UDI In Commercial Distribution 🇺🇸 United States

MICROFLEX

DI: 00769799205019 · Model: EV-2050-XS · Ansell Healthcare Product
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

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
MICROFLEX
Primary DI
00769799205019
Version / Model
EV-2050-XS
Catalog Number
EV-2050-XS
Company Name
Ansell Healthcare Product
Labeler DUNS
111267330
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2022-03-17
Public Version
2
Public Version Date
2026-04-08
Public Version Status
Update
Public Device Record Key
1ff80d17-797e-4f36-ac43-f73e354b52a7

Device Description

MICROFLEX EV-2050 EVOLUTION ONE SIZE XS (5.5-6.0), Latex Powder-Free Examination Glove

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYY Latex Patient Examination Glove

GMDN Terms

Code Name
47172 Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 00769799205064
Primary 00769799205019
Unit of Use 00071483002737

Customer Contacts

Phone
775-470-7106
Phone
7757466600