FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651795110 · Model: 79511 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
40

Basic Information

Brand Name
Halyard
Primary DI
10680651795110
Version / Model
79511
Catalog Number
79511
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2020-07-17
Public Version
3
Public Version Date
2021-11-01
Public Version Status
Update
Public Device Record Key
e0e4dafc-1242-4ac0-afcc-9856d92ab9fd

Device Description

HALYARD* ULTRA* SMS & Film Surgical Gown-Large-Handi-Bin-480

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
35091 Surgical gown, single-use

Identifiers

Type ID
Package 30680651795114
Primary 10680651795110
Unit of Use 90680651795116

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K842115 000