FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651476262 · Model: 47626 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10680651476262
Version / Model
47626
Catalog Number
47626
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-01
Public Version
1
Public Version Date
2019-07-09
Public Version Status
New
Public Device Record Key
9a8bcf64-16e8-4a13-853a-18f2f3d63ead

Device Description

HYH,R-FOLD,DRAPE,-,55X76,40

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
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 30680651476266
Primary 10680651476262

Customer Contacts