FDA UDI Not in Commercial Distribution 🇺🇸 United States

Halyard

DI: 20680651127369 · Model: 12736 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
48

Basic Information

Brand Name
Halyard
Primary DI
20680651127369
Version / Model
12736
Catalog Number
12736
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
48
Record Status
Published
Publish Date
2016-04-21
Public Version
6
Public Version Date
2023-01-02
Public Version Status
Update
Public Device Record Key
a632b0ab-0e7a-4b46-946f-acf7df1b8ea1
Distribution End Date
2023-01-01

Device Description

HYHL100 OS WRAP 36X36

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
FRG Wrap, sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package 30680651127366
Primary 20680651127369
Unit of Use 90680651127368

Customer Contacts