FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10809160345207 · Model: KDAU222-02_0006 · AVID MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10809160345207
Version / Model
KDAU222-02_0006
Catalog Number
KDAU222-02
Company Name
AVID MEDICAL, INC.
Labeler DUNS
015623119
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-09
Public Version
1
Public Version Date
2021-02-17
Public Version Status
New
Public Device Record Key
aa1ea589-6124-42a3-bdc5-d4211244ea17

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
OEZ Cardiovascular procedure kit

GMDN Terms

Code Name
46408 Cardiothoracic surgical procedure kit, medicated, single-use

Identifiers

Type ID
Package 20809160345204
Primary 10809160345207

Customer Contacts