FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040113100 · Model: 5701472 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
20

Basic Information

Brand Name
Henry Schein
Primary DI
10304040113100
Version / Model
5701472
Catalog Number
5701472
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2019-10-28
Public Version
2
Public Version Date
2021-08-24
Public Version Status
Update
Public Device Record Key
f86527ac-0219-495c-a6e5-d14310cb88ca

Device Description

Combine ABD Pad

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
48131 Non-woven gauze pad

Identifiers

Type ID
Package 20304040113107
Primary 10304040113100
Unit of Use 00304040113103