FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10885632416309 · Model: 55562 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10885632416309
Version / Model
55562
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-30
Public Version
1
Public Version Date
2024-08-07
Public Version Status
New
Public Device Record Key
08d5bbf2-7f7b-4bcf-8519-1e1a220ad148

Device Description

Film Dressing Transparent Sterile 4 X 4.75 Inch NonWoven CA/200 Not made with Natural Rubber Latex Halyard

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
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
KMK DEVICE, INTRAVASCULAR CATHETER SECUREMENT

GMDN Terms

Code Name
58301 Synthetic polymer semi-permeable film dressing, adhesive

Identifiers

Type ID
Package 20885632416306
Primary 10885632416309
Package 30885632416303