FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 30680651491184 · Model: 49118 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
Halyard
Primary DI
30680651491184
Version / Model
49118
Catalog Number
49118
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2023-11-15
Public Version
1
Public Version Date
2023-11-23
Public Version Status
New
Public Device Record Key
7ce56157-a702-4fbf-8b80-c2ae2ea5e145

Device Description

HYH,-,SRGDRP,BU,60X48,40

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PUI Drape, surgical, exempt

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Unit of Use 10680651491180
Primary 30680651491184

Customer Contacts