FDA UDI In Commercial Distribution 🇺🇸 United States

Pure Grip G2

DI: 10304040101909 · Model: 1125533 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
Pure Grip G2
Primary DI
10304040101909
Version / Model
1125533
Catalog Number
1125533
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2019-12-26
Public Version
2
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
6545bafd-158b-4151-a714-fbba07059cdf

Device Description

Pure Grip G2 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
Yes
Not Made with NRL
No
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 20304040101906
Primary 10304040101909
Unit of Use 00304040101919

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
FALSE