FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651426502 · Model: 42650 · O&M HALYARD, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10680651426502
Version / Model
42650
Catalog Number
42650-01 ACM
Company Name
O&M HALYARD, INC.
Labeler DUNS
081057389
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-10
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
496d36bf-e3b4-4c53-840c-2da89274b50a

Device Description

ACM,CARDIO,SRGDRP,-,XL,12

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 30680651426506
Primary 10680651426502

Customer Contacts