FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: H68010467081 · Model: 1046708 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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
Henry Schein
Primary DI
H68010467081
Version / Model
1046708
Catalog Number
1046708
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-31
Public Version
3
Public Version Date
2024-11-07
Public Version Status
Update
Public Device Record Key
a4c0312f-104a-47e4-aa5e-dd03a90c5cfa

Device Description

Conforming Stretch Gauze Sterile

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
No
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
Primary H68010467081