FDA UDI In Commercial Distribution 🇺🇸 United States

Criterion Aloe Advance Latex

DI: 10304040102050 · Model: 1125842 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Criterion Aloe Advance Latex
Primary DI
10304040102050
Version / Model
1125842
Catalog Number
1125842
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-01-08
Public Version
2
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
69cd8884-b01f-407f-b1b8-15ccf7a24c33

Device Description

Criterion Aloe Advance Latex Medium

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
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 20304040102057
Primary 10304040102050
Unit of Use 00304040102053

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
FALSE