FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651792287 · Model: 79228 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Halyard
Primary DI
10680651792287
Version / Model
79228
Catalog Number
79228
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-09-27
Public Version
1
Public Version Date
2019-10-07
Public Version Status
New
Public Device Record Key
692b46d2-a80b-46b7-b004-2be4b7ea3562

Device Description

HALYARD BASICS* Laparotomy Drape

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
Package 30680651792281
Primary 10680651792287
Unit of Use 90680651792283

Customer Contacts