FDA UDI In Commercial Distribution 🇺🇸 United States

Halyard

DI: 10680651391978 · Model: 39197 · Avanos Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Halyard
Primary DI
10680651391978
Version / Model
39197
Catalog Number
EL-2MTP
Company Name
Avanos Medical, Inc.
Labeler DUNS
079375431
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-30
Public Version
4
Public Version Date
2018-11-16
Public Version Status
Update
Public Device Record Key
b69f1c8c-e816-4d69-9149-be7fcbf41954

Device Description

HALYARD* Lead Set - 2 Feet

Device Characteristics

Single Use
No
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
KOI STIMULATOR, NERVE, PERIPHERAL, ELECTRIC

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 10680651391978

Customer Contacts