FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651355857 · Model: 35585 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10680651355857
Version / Model
35585
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-15
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
06b38091-63bd-411d-8458-7fa5b872f60d

Device Description

HYBRID CV / NUERO 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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 30680651355851
Primary 10680651355857

Customer Contacts