FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651796029 · Model: 79602 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
120

Basic Information

Brand Name
Halyard
Primary DI
30680651796029
Version / Model
79602
Catalog Number
79602
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
120
Record Status
Published
Publish Date
2019-12-04
Public Version
1
Public Version Date
2019-12-12
Public Version Status
New
Public Device Record Key
a34be8f3-1530-45dc-b9a9-abb8a1e99db3

Device Description

HALYARD* Standard Mayo Stand Cover-30 x 57-Handi-Bin-120-1-120-Regular

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
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47782 Patient surgical drape, single-use, non-sterile

Identifiers

Type ID
Primary 30680651796029
Unit of Use 90680651796021

Customer Contacts