FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040152055 · Model: 5702595 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Henry Schein
Primary DI
10304040152055
Version / Model
5702595
Catalog Number
5702595
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2021-04-23
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
3581c515-aaf1-4875-b489-68b20864a166

Device Description

Criterion Non-woven Sponges Sterile

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
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FRL FIBER, MEDICAL, ABSORBENT

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Package 20304040152052
Primary 10304040152055
Unit of Use 00304040152058