FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651449734 · Model: 44973 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
24

Basic Information

Brand Name
Halyard
Primary DI
30680651449734
Version / Model
44973
Catalog Number
44973
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
Record Status
Published
Publish Date
2016-06-15
Public Version
4
Public Version Date
2018-11-08
Public Version Status
Update
Public Device Record Key
098bb28d-9999-451c-8f76-d9ff38e15936

Device Description

CLEAR VIEW SCREEN NON-STERILE

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

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

Identifiers

Type ID
Primary 30680651449734
Unit of Use 90680651449736

Customer Contacts