FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10885632413933 · Model: 51794 · OWENS & MINOR DISTRIBUTION, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Halyard
Primary DI
10885632413933
Version / Model
51794
Company Name
OWENS & MINOR DISTRIBUTION, INC.
Labeler DUNS
007941230
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-04
Public Version
2
Public Version Date
2026-01-12
Public Version Status
Update
Public Device Record Key
66637f9f-ee89-46c0-bb99-23332ea6021a

Device Description

PERINEAL PACK EXTRA LONG 6X12.5IN UREA BLEND CA 24 WITH ADHESIVE STRIP SINGLE PT 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
No
Sterilization Prior Use
No

Product Codes

Code Name
IMD PACK, HOT OR COLD, DISPOSABLE

GMDN Terms

Code Name
40555 Musculoskeletal hot/cold therapy pack, single-use

Identifiers

Type ID
Package 20885632413930
Primary 10885632413933