FDA UDI In Commercial Distribution 🇺🇸 United States

Henry Schein

DI: 10304040185602 · Model: 5703818 · HENRY SCHEIN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

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Basic Information

Brand Name
Henry Schein
Primary DI
10304040185602
Version / Model
5703818
Catalog Number
5703818
Company Name
HENRY SCHEIN, INC.
Labeler DUNS
012430880
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2024-06-03
Public Version
1
Public Version Date
2024-06-11
Public Version Status
New
Public Device Record Key
6037423e-0f4f-44a7-b696-98e012052348

Device Description

Pack Angiography Drape F/Nevada Vein And Vascular

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Unit of Use 00304040185605
Primary 10304040185602